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: rs737337
rs737337
6 0.925 0.040 19 11236817 synonymous variant T/C snv 0.15 0.20 0.700 1.000 2 2010 2013
dbSNP: rs12979813
rs12979813
4 19 11232027 intron variant A/G snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs2278426
rs2278426
11 1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 0.700 1.000 1 2013 2013