| | CSMD1, LOC105377785 (V3563E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (A3532T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (N3527K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (N3520D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (R3514T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (H3481L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (Q3474H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (D3453G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (L3397V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (V3354I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (A3309T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (T3301S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (A3284T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (D3210G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (S3202N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (D3198H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (Q3180L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (R3165L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (Q3149H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (L3096V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (P3090T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (P3087L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (D3082H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (K3081N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (R3078L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (I3047M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (D3031N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (M3015I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (D2895Y) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (E2889K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (S2888G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (L2870V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (A2856G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (M2842V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (P2814S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (F2813L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (N2812Y) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (Q2811L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (T2766M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (N2757S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CSMD1, LOC105377785 (G2681D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377785, CSMD1 (S2621L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |