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: rs104894100
rs104894100
1 1.000 0.120 9 136673906 missense variant A/G snv 0.800 1.000 2 2002 2005
dbSNP: rs145975461
rs145975461
1 1.000 0.120 9 136673873 missense variant G/A;C snv 8.4E-04; 4.3E-06; 4.3E-06 0.700 1.000 2 2002 2005