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: rs16948048
rs16948048
3 0.925 0.040 17 49363104 intron variant A/G snv 0.37 0.700 1.000 2 2011 2011
dbSNP: rs12940887
rs12940887
2 17 49325445 intron variant C/T snv 0.28 0.700 1.000 1 2011 2011