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: rs10770125
rs10770125
4 0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 0.010 1.000 1 2017 2017
dbSNP: rs2585
rs2585
1 11 2129214 3 prime UTR variant T/C;G snv 0.010 1.000 1 2017 2017