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: rs1057519827
rs1057519827
2 6 152011697 missense variant G/C snv 0.700 1.000 3 2013 2014
dbSNP: rs1057519717
rs1057519717
1 6 152098785 missense variant T/G snv 0.700 1.000 2 2013 2013
dbSNP: rs1057519714
rs1057519714
1 6 152094402 missense variant T/C snv 0.700 1.000 1 2013 2013
dbSNP: rs1057519715
rs1057519715
2 1.000 0.080 6 152098779 missense variant T/A snv 0.700 1.000 1 2013 2013
dbSNP: rs1057519716
rs1057519716
1 6 152098782 missense variant C/A snv 0.700 1.000 1 2013 2013
dbSNP: rs796065354
rs796065354
9 0.882 0.080 6 151944320 missense variant A/G snv 0.040 1.000 4 2005 2009
dbSNP: rs1462893414
rs1462893414
5 0.882 0.080 6 151944323 missense variant A/G snv 4.0E-06 7.0E-06 0.030 1.000 3 2005 2007
dbSNP: rs904571820
rs904571820
5 0.851 0.160 6 151842664 start lost A/G snv 4.0E-06 0.010 1.000 1 2017 2017