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: rs772794204
rs772794204
1 1.000 0.120 2 206144934 missense variant A/C;G snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs774232299
rs774232299
1 1.000 0.120 2 206144019 missense variant A/G snv 4.0E-06 0.010 1.000 1 2010 2010