Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11554273
GNAS
0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 17
rs1057518907
GNAS
0.732 0.320 20 58891811 stop gained C/G;T snv 16
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 15
rs137854530
GNAS
0.776 0.240 20 58891727 start lost A/G;T snv 8