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: rs11920090
rs11920090
5 1.000 0.040 3 170999732 intron variant T/A snv 0.20 0.800 1.000 1 2012 2012
dbSNP: rs11924032
rs11924032
3 3 171017310 intron variant G/A snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs61791109
rs61791109
1 3 171016588 intron variant T/C snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs7356034
rs7356034
1 3 171014810 intron variant G/A snv 0.35 0.700 1.000 1 2019 2019