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: rs3219090
rs3219090
1 1.000 0.040 1 226376990 intron variant T/C snv 0.58 0.820 1.000 2 2011 2013
dbSNP: rs1136410
rs1136410
70 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2006 2006
dbSNP: rs3219125
rs3219125
1 1.000 0.040 1 226367250 non coding transcript exon variant T/C snv 5.0E-02 0.010 1.000 1 2011 2011