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: rs1344555
rs1344555
4 3 169582431 intron variant C/A;G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs78101726
rs78101726
2 3 169577648 intron variant A/G snv 0.16 0.700 1.000 1 2019 2019