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: rs7412
rs7412
47 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.800 1.000 12 2010 2019
dbSNP: rs405509
rs405509
30 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 0.700 1.000 3 2012 2013
dbSNP: rs429358
rs429358
66 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 2 2018 2018
dbSNP: rs769449
rs769449
11 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 0.700 1.000 2 2018 2019
dbSNP: rs769450
rs769450
5 0.925 0.120 19 44907187 non coding transcript exon variant G/A snv 0.39 0.700 1.000 2 2012 2012
dbSNP: rs769446
rs769446
6 0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs769455
rs769455
8 0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 0.700 1.000 1 2014 2014