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: rs28607014
rs28607014
1 1.000 0.040 12 117270806 intron variant C/T snv 0.32 0.700 1.000 2 2017 2019
dbSNP: rs2293052
rs2293052
2 1.000 0.040 12 117277815 intron variant G/A snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs6490121
rs6490121
1 1.000 0.040 12 117270390 intron variant G/A snv 0.64 0.060 1.000 6 2009 2018
dbSNP: rs3782206
rs3782206
1 1.000 0.040 12 117307284 intron variant C/T snv 0.11 0.030 1.000 3 2008 2017
dbSNP: rs41279104
rs41279104
6 0.827 0.160 12 117439680 intron variant C/T snv 0.11 0.030 1.000 3 2011 2019
dbSNP: rs2682826
rs2682826
11 0.807 0.280 12 117215033 3 prime UTR variant G/A snv 0.25 0.010 1.000 1 2009 2009
dbSNP: rs499776
rs499776
1 1.000 0.040 12 117341694 intron variant G/A snv 0.35 0.010 1.000 1 2017 2017