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: rs11090910
rs11090910
3 0.882 0.080 22 46111790 non coding transcript exon variant T/C snv 0.30 0.010 1.000 1 2015 2015
dbSNP: rs11703832
rs11703832
3 0.882 0.080 22 46108287 intron variant C/T snv 0.19 0.010 1.000 1 2015 2015
dbSNP: rs12170325
rs12170325
3 0.882 0.080 22 46106990 intron variant C/T snv 0.18 0.010 1.000 1 2015 2015
dbSNP: rs13053856
rs13053856
3 0.882 0.080 22 46104002 intron variant G/A;T snv 0.010 1.000 1 2015 2015