Source: INFERRED ×
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: rs4369779
rs4369779
1 18 23155444 intron variant T/A;C snv 0.700 1.000 5 2014 2019
dbSNP: rs4800148
rs4800148
4 18 23144364 intron variant G/A;C snv 0.700 1.000 3 2008 2019
dbSNP: rs11082304
rs11082304
6 18 23141009 intron variant G/C;T snv 0.700 1.000 2 2013 2019
dbSNP: rs4800452
rs4800452
3 18 23147647 intron variant C/G;T snv 0.700 1.000 2 2010 2019
dbSNP: rs34302357
rs34302357
1 18 23178346 intron variant A/G snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs8096254
rs8096254
1 18 23133251 upstream gene variant G/A;C snv 0.700 1.000 1 2017 2017