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: rs4565845
rs4565845
1 1.000 0.040 10 122399534 intron variant A/C snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs4751890
rs4751890
1 1.000 0.040 10 122402275 intron variant T/C snv 0.31 0.700 1.000 1 2013 2013
dbSNP: rs6585827
rs6585827
3 1.000 0.040 10 122406099 intron variant G/A snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs7072204
rs7072204
2 0.925 0.120 10 122435969 3 prime UTR variant A/G snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs7079976
rs7079976
1 1.000 0.040 10 122412592 non coding transcript exon variant A/G snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs7084349
rs7084349
1 1.000 0.040 10 122385624 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs7097701
rs7097701
1 1.000 0.040 10 122412341 non coding transcript exon variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs7902176
rs7902176
1 1.000 0.040 10 122387175 5 prime UTR variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs8181474
rs8181474
1 1.000 0.040 10 122401065 intron variant G/A snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs4612730
rs4612730
1 1.000 0.040 10 122416936 intron variant G/A snv 0.47 0.47 0.700 1.000 1 2013 2013