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: rs11684176
rs11684176
3 2 198090050 intron variant C/T snv 0.38 0.700 1.000 1 2016 2016
dbSNP: rs1595824
rs1595824
3 2 198009282 intron variant C/A;T snv 0.700 1.000 1 2016 2016