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: rs1275980031
rs1275980031
2 1.000 0.040 7 103540259 missense variant G/A snv 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs362691
rs362691
3 0.882 0.120 7 103610714 missense variant G/A;C;T snv 1.2E-05; 0.12 0.010 1.000 1 2014 2014
dbSNP: rs7341475
rs7341475
6 0.851 0.240 7 103764368 intron variant G/A snv 0.17 0.010 1.000 1 2017 2017
dbSNP: rs736707
rs736707
6 0.851 0.040 7 103489956 intron variant A/G snv 0.30 0.010 1.000 1 2014 2014