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: rs932764
rs932764
6 10 94136183 intron variant A/G snv 0.38 0.700 1.000 4 2011 2017
dbSNP: rs10882397
rs10882397
2 10 94132902 intron variant C/A snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs11187838
rs11187838
3 10 94278929 non coding transcript exon variant G/A snv 0.44 0.700 1.000 1 2019 2019
dbSNP: rs57866767
rs57866767
1 10 94263320 intron variant T/C snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs7080472
rs7080472
1 10 94253193 intron variant G/A;T snv 0.700 1.000 1 2018 2018