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: rs11613352
rs11613352
9 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.800 1.000 4 2010 2018
dbSNP: rs540730
rs540730
3 12 57413331 intron variant T/C snv 0.71 0.700 1.000 2 2018 2019