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: rs11191580
rs11191580
13 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 0.700 1.000 1 2013 2013
dbSNP: rs11191582
rs11191582
2 1.000 0.040 10 103153896 intron variant G/A snv 7.7E-02 0.700 1.000 1 2017 2017