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: rs9383938
rs9383938
2 0.827 0.160 6 151666222 intron variant G/T snv 0.11 0.720 1.000 1 2011 2014
dbSNP: rs2747652
rs2747652
1 1.000 0.080 6 152115881 intron variant T/C snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs6904031
rs6904031
1 1.000 0.080 6 151734843 intron variant A/T snv 9.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs78796841
rs78796841
1 1.000 0.080 6 151859461 intron variant A/G snv 1.6E-02 0.700 1.000 1 2017 2017