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: rs11666808
rs11666808
3 1.000 0.040 19 18272696 intron variant T/C snv 0.67 0.700 1.000 1 2019 2019