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: rs11038167
rs11038167
1 1.000 0.040 11 44821583 intron variant A/C;G snv 0.840 0.750 1 2011 2017
dbSNP: rs11038172
rs11038172
1 1.000 0.040 11 44834046 intron variant A/G snv 5.1E-02 0.730 1.000 1 2011 2016
dbSNP: rs835784
rs835784
1 1.000 0.040 11 44842267 intron variant A/G snv 0.52 0.720 1.000 1 2011 2013