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: rs6740584
rs6740584
4 0.882 0.040 2 207564627 intron variant T/C snv 0.37 0.020 1.000 2 2013 2017
dbSNP: rs11904814
rs11904814
5 0.851 0.080 2 207562074 intron variant T/G snv 0.30 0.010 1.000 1 2017 2017
dbSNP: rs2254137
rs2254137
2 0.925 0.040 2 207579304 intron variant C/A snv 0.57 0.010 1.000 1 2013 2013
dbSNP: rs2551922
rs2551922
1 1.000 0.040 2 207573836 intron variant A/G snv 0.87 0.010 1.000 1 2013 2013
dbSNP: rs6785
rs6785
4 0.851 0.120 2 207603273 3 prime UTR variant A/G snv 0.84 0.010 < 0.001 1 2018 2018