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: rs3132680
rs3132680
1 1.000 0.120 6 30105418 non coding transcript exon variant A/C snv 0.73 0.700 1.000 2 2007 2009
dbSNP: rs4959041
rs4959041
2 0.925 0.120 6 30110190 intron variant T/C snv 0.29 0.700 1.000 2 2007 2009
dbSNP: rs2523990
rs2523990
1 1.000 0.120 6 30109452 intron variant A/G snv 0.43 0.700 1.000 1 2007 2007
dbSNP: rs2844795
rs2844795
5 0.925 0.120 6 30106070 intron variant C/G;T snv 0.700 1.000 1 2009 2009