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: rs11643630
rs11643630
2 0.925 0.080 16 55476547 intron variant T/G snv 0.55 0.010 1.000 1 2009 2009
dbSNP: rs11644561
rs11644561
2 0.925 0.080 16 55475122 intron variant G/A snv 0.20 0.010 1.000 1 2009 2009
dbSNP: rs2285053
rs2285053
15 0.752 0.320 16 55478465 intron variant C/T snv 0.12 0.010 1.000 1 2019 2019