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: rs7173419
rs7173419
1 15 27951675 intron variant T/C snv 0.60 0.800 1.000 1 2013 2013
dbSNP: rs11855019
rs11855019
2 15 28090674 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs7495174
rs7495174
3 15 28099092 intron variant A/G snv 0.12 0.700 1.000 1 2013 2013
dbSNP: rs76930569
rs76930569
1 15 27950999 intron variant C/T snv 1.4E-02 0.700 1.000 1 2017 2017