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: rs10865879
rs10865879
1 3 38535871 intron variant A/C snv 0.21 0.700 1.000 1 2016 2016
dbSNP: rs2051211
rs2051211
1 3 38518258 intron variant A/C;G snv 0.23 0.700 1.000 1 2016 2016