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: rs10753933
rs10753933
1 1.000 0.080 1 203057086 intron variant T/G snv 0.47 0.700 1.000 2 2018 2018
dbSNP: rs17461925
rs17461925
1 1.000 0.080 1 203057463 intron variant A/G snv 0.41 0.700 1.000 1 2017 2017
dbSNP: rs3737883
rs3737883
1 1.000 0.080 1 203065778 intron variant A/G snv 0.47 0.700 1.000 1 2017 2017
dbSNP: rs4590732
rs4590732
1 1.000 0.080 1 203059583 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11579055
rs11579055
1 1.000 0.080 1 203062187 intron variant G/T snv 0.47 0.010 1.000 1 2017 2017