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: rs11819869
rs11819869
1 1.000 0.040 11 46539130 intron variant C/T snv 0.27 0.710 1.000 1 2012 2013
dbSNP: rs12574668
rs12574668
1 1.000 0.040 11 46401136 intron variant C/A snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs7112229
rs7112229
1 1.000 0.040 11 46491699 intron variant C/T snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs7130141
rs7130141
1 1.000 0.040 11 46478324 intron variant C/T snv 0.27 0.700 1.000 1 2012 2012