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: rs10275045
rs10275045
2 0.882 0.160 7 1881190 intron variant C/T snv 0.35 0.700 1.000 1 2014 2014
dbSNP: rs3931398
rs3931398
1 1.000 0.040 7 1991957 intron variant G/A snv 0.700 1.000 1 2018 2018
dbSNP: rs4236274
rs4236274
1 1.000 0.040 7 1856777 intron variant A/G snv 0.47 0.700 1.000 1 2016 2016
dbSNP: rs4332037
rs4332037
1 1.000 0.040 7 1911173 intron variant C/T snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs4721295
rs4721295
3 0.882 0.040 7 1997034 intron variant T/G snv 0.33 0.700 1.000 1 2013 2013