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: rs191486604
rs191486604
2 0.923 0.036 6 161350208 missense variant C/T snp 6.0E-05 1.3E-04 0.700 11 2000 2016
dbSNP: rs34424986
rs34424986
8 0.784 0.107 6 161785820 missense variant G/A,T snp 1.9E-03; 8.0E-06 2.3E-03 0.700 10 1999 2016
dbSNP: rs121918227
rs121918227
2 0.923 0.036 1 16996008 missense variant C/G snp 0.010 1.000 1 2007 2007