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: rs755287627
rs755287627
1 1.000 0.120 4 113353494 missense variant A/G snv 4.0E-06 0.700 0
dbSNP: rs796052197
rs796052197
1 1.000 0.120 4 113354767 missense variant T/C snv 0.700 0
dbSNP: rs796052198
rs796052198
1 1.000 0.120 4 113356741 missense variant T/C snv 0.700 0
dbSNP: rs1408198357
rs1408198357
1 1.000 0.120 4 113373391 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 1998 1998