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: rs116840778
rs116840778
7 0.882 0.200 3 8733956 missense variant G/A;C snv 0.800 0
dbSNP: rs116840786
rs116840786
1 3 8733962 missense variant C/A;T snv 0.800 0
dbSNP: rs116840789
rs116840789
6 0.925 0.080 3 8745547 missense variant G/A;T snv 0.700 0
dbSNP: rs116840795
rs116840795
2 1.000 0.120 3 8745580 missense variant G/A snv 1.2E-05 7.0E-06 0.700 0