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: rs10036748
rs10036748
11 0.752 0.360 5 151078585 intron variant C/A;T snv 0.710 1.000 2 2015 2019
dbSNP: rs2233278
rs2233278
2 0.925 0.040 5 151087628 5 prime UTR variant G/C;T snv 4.8E-02 0.800 1.000 2 2012 2015
dbSNP: rs3762999
rs3762999
1 1.000 0.040 5 151089865 intron variant C/T snv 0.49 0.700 1.000 1 2010 2010
dbSNP: rs74817271
rs74817271
6 0.807 0.120 5 151090412 intron variant G/A snv 5.0E-02 0.700 1.000 1 2016 2016