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: rs2279463
rs2279463
4 1.000 0.080 6 160247357 intron variant A/G;T snv 0.700 1.000 4 2010 2019
dbSNP: rs3127573
rs3127573
2 6 160260361 5 prime UTR variant A/G snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs316009
rs316009
2 6 160254732 intron variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs316020
rs316020
2 6 160248049 intron variant A/G snv 0.89 0.700 1.000 1 2018 2018