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: rs1475170339
rs1475170339
18 0.732 0.240 16 1792325 missense variant T/C;G snv 0.100 1.000 10 1999 2009
dbSNP: rs1410835752
rs1410835752
2 0.925 0.080 16 1792440 missense variant G/A snv 0.030 1.000 3 1994 2000
dbSNP: rs1226535830
rs1226535830
2 0.925 0.080 16 1792123 missense variant T/C snv 4.2E-06 0.010 1.000 1 2011 2011
dbSNP: rs1420149251
rs1420149251
2 0.925 0.080 16 1792441 missense variant C/A;T snv 0.010 1.000 1 1996 1996
dbSNP: rs759097092
rs759097092
2 0.925 0.080 16 1792237 missense variant T/C snv 8.5E-06 0.010 1.000 1 2011 2011