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: rs11079725
rs11079725
3 0.925 0.120 17 45846568 synonymous variant T/C snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs111972148
rs111972148
1 1.000 0.080 17 45895755 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs113161176
rs113161176
1 1.000 0.080 17 45896988 non coding transcript exon variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs113347741
rs113347741
1 1.000 0.080 17 45896042 non coding transcript exon variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs11575895
rs11575895
1 1.000 0.080 17 45894419 5 prime UTR variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs11575896
rs11575896
1 1.000 0.080 17 45894776 non coding transcript exon variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12185233
rs12185233
4 0.882 0.160 17 45846288 missense variant G/A;C snv 9.5E-05; 0.15 0.700 1.000 1 2012 2012
dbSNP: rs12185268
rs12185268
5 0.851 0.160 17 45846317 missense variant A/G snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12373123
rs12373123
4 0.882 0.160 17 45846707 missense variant T/C snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12373124
rs12373124
9 0.790 0.120 17 45846853 synonymous variant T/C snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12373139
rs12373139
4 0.925 0.120 17 45846764 missense variant G/A snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12373140
rs12373140
1 1.000 0.080 17 45846865 synonymous variant G/A snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12373142
rs12373142
5 0.851 0.200 17 45846834 missense variant C/G;T snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs17690679
rs17690679
3 0.925 0.120 17 45847437 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17690703
rs17690703
4 0.882 0.160 17 45847931 intron variant C/T snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs17763515
rs17763515
1 1.000 0.080 17 45840452 intron variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17763533
rs17763533
2 1.000 0.080 17 45840824 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17763596
rs17763596
3 0.925 0.120 17 45843844 non coding transcript exon variant G/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17769490
rs17769490
3 0.925 0.120 17 45848239 intron variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17769552
rs17769552
3 0.925 0.120 17 45849924 intron variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs34416056
rs34416056
1 1.000 0.080 17 45873854 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs55943825
rs55943825
1 1.000 0.080 17 45847410 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs56150806
rs56150806
1 1.000 0.080 17 45841935 non coding transcript exon variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs56385754
rs56385754
1 1.000 0.080 17 45849889 intron variant G/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs62054820
rs62054820
1 1.000 0.080 17 45849389 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012