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: rs121434569
rs121434569
29 0.667 0.321 7 55181378 missense variant C/T snp 2.8E-05 9.6E-05 0.040 1.000 4 2007 2016
dbSNP: rs121434568
rs121434568
33 0.642 0.321 7 55191822 missense variant T/A,G snp 0.010 < 0.001 1 2012 2012
dbSNP: rs723526
rs723526
3 0.923 0.036 7 55067126 intron variant A/G snp 0.86 0.010 1.000 1 2013 2013