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: rs137853165
rs137853165
STS
1 1.000 0.120 X 7325356 missense variant T/A snv 0.800 1.000 4 1992 2000
dbSNP: rs137853166
rs137853166
STS
1 1.000 0.120 X 7334066 missense variant G/A snv 0.800 1.000 4 1992 2000
dbSNP: rs137853167
rs137853167
STS
1 1.000 0.120 X 7305109 missense variant C/T snv 0.800 1.000 4 1992 2000
dbSNP: rs137853168
rs137853168
STS
1 1.000 0.120 X 7325357 missense variant G/C snv 0.800 1.000 4 1992 2000
dbSNP: rs137853169
rs137853169
STS
1 1.000 0.120 X 7334060 missense variant A/G snv 0.800 1.000 4 1992 2000