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: rs11130317
rs11130317
1 1.000 0.040 3 52697467 intron variant C/T snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs12635140
rs12635140
2 0.925 0.040 3 52704149 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs2164885
rs2164885
1 1.000 0.040 3 52697253 intron variant T/C snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs3733041
rs3733041
2 0.925 0.040 3 52697582 intron variant T/C snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs3755798
rs3755798
2 0.925 0.040 3 52707144 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs6976
rs6976
4 0.851 0.080 3 52694788 3 prime UTR variant C/T snv 0.38 0.33 0.700 1.000 1 2013 2013
dbSNP: rs8906
rs8906
1 1.000 0.040 3 52705504 5 prime UTR variant T/C snv 0.33 0.700 1.000 1 2013 2013