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: rs11152369
rs11152369
5 0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 0.700 1.000 1 2013 2013
dbSNP: rs12954356
rs12954356
2 1.000 0.040 18 55586179 5 prime UTR variant G/C snv 1.8E-03 0.700 1.000 1 2017 2017
dbSNP: rs9636107
rs9636107
3 1.000 0.040 18 55532886 intron variant A/G;T snv 0.700 1.000 1 2017 2017