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: rs62637014
rs62637014
2 0.925 0.040 17 6425781 stop gained C/T snv 3.3E-04 3.8E-04 0.700 1.000 2 2000 2019
dbSNP: rs142326926
rs142326926
1 1.000 0.040 17 6426615 missense variant C/T snv 3.2E-05 4.9E-05 0.700 0
dbSNP: rs62637010
rs62637010
1 1.000 0.040 17 6426934 missense variant C/G snv 0.700 0
dbSNP: rs62637011
rs62637011
1 1.000 0.040 17 6426906 missense variant A/T snv 0.700 0
dbSNP: rs62637012
rs62637012
2 0.925 0.040 17 6426684 missense variant A/G snv 0.700 0