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: rs104894077
rs104894077
8 0.790 0.080 8 74361886 stop gained C/T snv 7.6E-05 1.5E-04 0.700 0
dbSNP: rs104894078
rs104894078
5 0.851 0.080 8 74360184 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs281865060
rs281865060
2 0.925 0.080 8 74360173 missense variant T/C;G snv 8.0E-06 7.0E-06 0.700 0