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: rs6352
rs6352
2 0.925 0.040 17 30203175 missense variant T/G snv 6.6E-03 4.4E-03 0.010 1.000 1 2006 2006
dbSNP: rs7224199
rs7224199
7 0.827 0.160 17 30196708 3 prime UTR variant G/T snv 0.49 0.010 1.000 1 2020 2020