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: rs11694842
rs11694842
2 2 25260101 intron variant A/G snv 0.22 0.700 1.000 2 2015 2019
dbSNP: rs13427672
rs13427672
1 2 25250442 intron variant G/A snv 0.43 0.700 1.000 2 2017 2019
dbSNP: rs2289195
rs2289195
2 1.000 0.040 2 25240614 intron variant G/A snv 0.41 0.41 0.700 1.000 1 2014 2014
dbSNP: rs79478703
rs79478703
1 2 25235984 intron variant A/G snv 4.8E-02 0.700 1.000 1 2017 2017