Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1764390
rs1764390
GJA4 ; SMIM12 ; LOC105378642
3 0.882 0.160 1 34794360 missense variant A/C;G;T snv 0.61 0.69 0.010 1.000 1 2017 2017