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: rs17826816
rs17826816
2 1.000 0.040 5 7519185 intron variant A/G snv 0.17 0.800 1.000 1 2014 2014
dbSNP: rs10512928
rs10512928
1 1.000 0.040 5 7546298 intron variant C/T snv 0.15 0.700 1.000 1 2014 2014
dbSNP: rs11948030
rs11948030
1 1.000 0.040 5 7493064 intron variant T/C snv 0.15 0.700 1.000 1 2014 2014
dbSNP: rs12519539
rs12519539
1 1.000 0.040 5 7583043 intron variant A/G snv 0.15 0.700 1.000 1 2014 2014
dbSNP: rs12522444
rs12522444
1 1.000 0.040 5 7553388 intron variant G/A snv 0.15 0.700 1.000 1 2014 2014
dbSNP: rs13166360
rs13166360
1 1.000 0.040 5 7520768 missense variant G/A;C;T snv 0.18 0.18 0.700 1.000 1 2014 2014
dbSNP: rs17231202
rs17231202
1 1.000 0.040 5 7546174 intron variant A/G snv 0.15 0.700 1.000 1 2014 2014
dbSNP: rs17826395
rs17826395
1 1.000 0.040 5 7502943 intron variant A/C snv 0.16 0.700 1.000 1 2014 2014
dbSNP: rs4530734
rs4530734
1 1.000 0.040 5 7565039 intron variant G/T snv 0.15 0.700 1.000 1 2014 2014
dbSNP: rs58502974
rs58502974
2 0.925 0.040 5 7755787 intron variant T/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs884964
rs884964
1 1.000 0.040 5 7548741 intron variant T/C snv 0.21 0.700 1.000 1 2014 2014