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: rs11191548
rs11191548
10 0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 0.700 1.000 3 2011 2018
dbSNP: rs943037
rs943037
2 10 103076162 synonymous variant C/T snv 0.12 8.3E-02 0.700 1.000 1 2016 2016