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: rs10491279
rs10491279
1 1.000 0.071 5 132862408 synonymous variant C/T snp 0.14 0.17 0.010 1.000 1 2010 2010
dbSNP: rs76349024
rs76349024
1 1.000 0.071 5 132862518 missense variant G/A snp 3.4E-04 1.6E-04 0.010 1.000 1 2014 2014