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: rs2714337
rs2714337
2 6 7240344 intron variant A/T snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs35742417
rs35742417
2 1.000 0.080 6 7247111 missense variant C/A;G;T snv 0.13; 3.0E-04; 4.0E-06 0.700 1.000 1 2015 2015