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: rs11693031
rs11693031
2 1.000 0.040 2 211813206 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs62183032
rs62183032
2 1.000 0.040 2 211774137 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs72948529
rs72948529
1 1.000 0.040 2 211777265 non coding transcript exon variant A/C snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs74338595
rs74338595
2 1.000 0.040 2 211885061 intron variant T/C snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs7583068
rs7583068
2 1.000 0.040 2 211769383 intron variant T/A snv 0.33 0.700 1.000 1 2018 2018