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: rs7495132
rs7495132
10 0.790 0.080 15 90629669 intron variant C/T snv 0.12 0.800 1.000 2 2012 2017
dbSNP: rs7165170
rs7165170
2 1.000 0.040 15 90638257 non coding transcript exon variant A/C snv 0.26 0.700 1.000 1 2015 2015