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: rs10937405
rs10937405
9 0.807 0.080 3 189665394 intron variant C/T snv 0.38 0.840 1.000 5 2010 2014
dbSNP: rs13314271
rs13314271
2 0.925 0.080 3 189639813 intron variant T/C snv 0.45 0.710 1.000 1 2014 2014
dbSNP: rs11375254
rs11375254
3 0.882 0.080 3 189625454 intergenic variant A/-;AA;AAA;AAAA delins 0.700 1.000 1 2019 2019
dbSNP: rs13080835
rs13080835
2 0.925 0.080 3 189639410 intron variant G/T snv 0.45 0.700 1.000 1 2017 2017
dbSNP: rs7636839
rs7636839
1 1.000 0.040 3 189639152 intron variant A/G snv 0.45 0.700 1.000 1 2016 2016
dbSNP: rs4488809
rs4488809
5 0.827 0.080 3 189638472 intron variant T/C snv 0.45 0.010 1.000 1 2014 2014
dbSNP: rs6790167
rs6790167
5 0.827 0.080 3 189869485 intron variant A/G snv 0.53 0.010 1.000 1 2016 2016