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: rs1294404368
rs1294404368
1 1.000 0.080 7 98981947 missense variant C/T snv 4.4E-06 1.4E-05 0.700 0
dbSNP: rs373632999
rs373632999
1 1.000 0.080 7 98949733 missense variant G/A snv 1.2E-05 4.2E-05 0.700 0
dbSNP: rs528967912
rs528967912
1 1.000 0.080 7 98964724 missense variant C/T snv 1.6E-05 7.0E-06 0.700 0