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: rs10774021
rs10774021
4 1.000 0.080 12 240132 intron variant C/T snv 0.57 0.700 1.000 2 2010 2016
dbSNP: rs11062167
rs11062167
2 12 255573 intron variant G/A snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs67523949
rs67523949
1 12 239340 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019