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: rs950169
rs950169
1 1.000 0.040 15 84037709 missense variant C/T snv 0.22 0.19 0.800 1.000 1 2009 2019
dbSNP: rs2135551
rs2135551
1 1.000 0.040 15 84039099 3 prime UTR variant A/G snv 0.19 0.700 1.000 1 2009 2009