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: rs137852643
rs137852643
3 0.925 0.080 7 30609729 missense variant G/C snv 4.0E-06 0.700 1.000 6 2006 2016
dbSNP: rs1554338262
rs1554338262
1 1.000 0.080 7 30612215 missense variant T/A snv 0.700 1.000 3 2006 2014
dbSNP: rs1060502838
rs1060502838
2 0.925 0.080 7 30621448 missense variant A/G snv 0.700 1.000 2 2005 2014
dbSNP: rs1064795123
rs1064795123
1 1.000 0.080 7 30609724 missense variant T/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs1060502839
rs1060502839
1 1.000 0.080 7 30628565 missense variant G/A snv 0.700 0
dbSNP: rs1554337974
rs1554337974
3 0.882 0.080 7 30609643 missense variant C/T snv 0.700 0
dbSNP: rs1554338260
rs1554338260
2 0.925 0.080 7 30612214 missense variant A/T snv 0.700 0