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: rs7526762
rs7526762
2 1 74527634 intron variant A/G snv 0.42 0.700 1.000 1 2017 2017
dbSNP: rs7551507
rs7551507
2 1 74529541 intron variant C/T snv 0.41 0.700 1.000 1 2017 2017