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: rs11169552
rs11169552
10 0.776 0.080 12 50761880 upstream gene variant C/T snv 0.23 0.700 1.000 1 2010 2010
dbSNP: rs12372718
rs12372718
10 0.776 0.080 12 50777307 intron variant A/G snv 0.35 0.700 1.000 1 2019 2019