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: rs4765127
rs4765127
3 12 123975620 intron variant G/T snv 0.33 0.800 1.000 3 2010 2018
dbSNP: rs11057408
rs11057408
1 12 123980289 intron variant G/T snv 0.33 0.700 1.000 1 2017 2017
dbSNP: rs12310367
rs12310367
1 12 124002131 intron variant A/G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs7307277
rs7307277
2 12 123990609 intron variant A/G snv 0.32 0.700 1.000 1 2018 2018