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: rs429358
rs429358
39 0.630 0.321 19 44908684 missense variant T/C snp 0.14 0.16 0.820 1.000 4 2011 2015
dbSNP: rs769449
rs769449
7 0.878 0.107 19 44906745 non coding transcript exon variant G/A snp 9.1E-02 0.800 1 2013 2013
dbSNP: rs405509
rs405509
17 0.744 0.286 19 44905579 intergenic variant T/G snp 0.58 0.740 1.000 12 2009 2017
dbSNP: rs7259620
rs7259620
1 1.000 0.071 19 44904531 intergenic variant G/A,C snp 0.45 0.700 1 2013 2013
dbSNP: rs761592007
rs761592007
4 0.878 0.143 19 44909013 G/A snp 1.5E-05 0.020 1.000 2 2000 2012
dbSNP: rs11542041
rs11542041
19 0.707 0.357 19 44908690 missense variant C/T snp 6.4E-05 0.010 < 0.001 1 2009 2009
dbSNP: rs449647
rs449647
2 0.923 0.107 19 44905307 intergenic variant A/T snp 0.21 0.010 1.000 1 2009 2009
dbSNP: rs533904656
rs533904656
1 1.000 0.071 19 44907768 missense variant G/A,C snp 1.8E-04; 8.2E-06 1.3E-04 0.010 1.000 1 2008 2008
dbSNP: rs7412
rs7412
40 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.010 1.000 1 2011 2011
dbSNP: rs752600356
rs752600356
3 0.878 0.107 19 44908681 missense variant G/A snp 2.3E-05 0.010 1.000 1 2007 2007
dbSNP: rs769446
rs769446
4 0.878 0.107 19 44905371 intergenic variant T/C snp 7.1E-02 0.010 1.000 1 2009 2009