Related gene-specific medical variations for Gene (Select 5275) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2612574	NM_012397.4(SERPINB13):c.148G>T (p.Ala50Ser)	LOC126862774, SERPINB13 (A50S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524859	NM_012397.4(SERPINB13):c.106A>T (p.Thr36Ser)	LOC126862774, SERPINB13 (T36S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366958	NM_012397.4(SERPINB13):c.221A>T (p.Glu74Val)	LOC126862774, SERPINB13 (E74V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2348378	NM_012397.4(SERPINB13):c.188C>T (p.Thr63Met)	LOC126862774, SERPINB13 (T63M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2232142	NM_012397.4(SERPINB13):c.148G>C (p.Ala50Pro)	LOC126862774, SERPINB13 (A50P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 788137	NM_012397.4(SERPINB13):c.189G>A (p.Thr63=)	LOC126862774, SERPINB13	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

ClinVar