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: rs6470745
rs6470745
3 0.882 0.040 8 129629675 intron variant A/G snv 0.18 0.720 1.000 4 2009 2019
dbSNP: rs10464870
rs10464870
3 0.882 0.040 8 129465577 intron variant C/T snv 0.80 0.700 1.000 2 2009 2011
dbSNP: rs16904140
rs16904140
1 1.000 0.040 8 129653397 intron variant G/A snv 0.19 0.700 1.000 2 2009 2011
dbSNP: rs12544799
rs12544799
1 1.000 0.040 8 129651264 intron variant A/G snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs4636162
rs4636162
1 1.000 0.040 8 129627294 non coding transcript exon variant G/A snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs6985166
rs6985166
1 1.000 0.040 8 129666930 intron variant A/G snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs9656979
rs9656979
1 1.000 0.040 8 129652161 intron variant T/C snv 0.37 0.700 1.000 1 2011 2011
dbSNP: rs55705857
rs55705857
16 0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 0.760 1.000 9 2013 2019
dbSNP: rs891835
rs891835
5 0.851 0.120 8 129479506 intron variant T/G snv 0.17 0.810 1.000 3 2009 2019
dbSNP: rs4295627
rs4295627
11 0.763 0.200 8 129673211 intron variant T/G snv 0.17 0.900 1.000 12 2009 2020