Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1553650442
rs1553650442
0.925 0.160 2 178593732 frameshift variant C/-;CCC delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 14 1991 2014
dbSNP: rs1553650442
rs1553650442
0.925 0.160 2 178593732 frameshift variant C/-;CCC delins
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J
0.700 1.000 1 2015 2015
dbSNP: rs1553650442
rs1553650442
0.925 0.160 2 178593732 frameshift variant C/-;CCC delins
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g
0.700 1.000 1 2015 2015