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: rs2515895
rs2515895
1 1.000 0.040 6 32661183 intron variant T/C snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs2854272
rs2854272
1 1.000 0.040 6 32661903 non coding transcript exon variant A/G snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs4988888
rs4988888
1 1.000 0.040 6 32667420 intron variant T/C snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs9282114
rs9282114
1 1.000 0.040 6 32661903 non coding transcript exon variant -/C ins 0.700 1.000 1 2012 2012