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: rs4466998
rs4466998
1 14 65008822 intron variant C/A;G snv 0.800 1.000 1 2009 2009
dbSNP: rs11627485
rs11627485
5 14 65020976 intron variant T/C snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs7155454
rs7155454
2 14 65035521 intron variant G/A snv 0.61 0.700 1.000 1 2017 2017