| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FSIP1, LOC126862111 (L484V) | Single nucleotide variant (missense variant) | not specified | |
| | FSIP1, LOC126862111 (M493V) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FSIP1, LOC126862111 (L549F) | Single nucleotide variant (missense variant) | not specified | |
| | FSIP1, LOC126862111 (E562K) | Single nucleotide variant (missense variant) | not specified | |
| | FSIP1, LOC126862111 (M493L) | Single nucleotide variant (missense variant) | not specified | |
| | FSIP1, LOC126862111 (E414A) | Single nucleotide variant (missense variant) | not specified | |
| | FSIP1, LOC126862111 (F537L) | Single nucleotide variant (missense variant) | not specified | |
| | FSIP1, LOC126862111 (A478T) | Single nucleotide variant (missense variant) | not specified | |
| | FSIP1, LOC126862111 (P561L) | Single nucleotide variant (missense variant) | not specified | |
| | FSIP1, LOC126862111 (P541A) | Single nucleotide variant (missense variant) | not specified | |
Click to view in NCBI Gene