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: rs76324150
rs76324150
1 1.000 0.080 17 45895867 non coding transcript exon variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs74548327
rs74548327
1 1.000 0.080 17 45895714 intron variant A/G 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: 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: rs55943825
rs55943825
1 1.000 0.080 17 45847410 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
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: rs62056782
rs62056782
1 1.000 0.080 17 45896864 non coding transcript exon variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs80233201
rs80233201
1 1.000 0.080 17 45894115 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: rs62056778
rs62056778
1 1.000 0.080 17 45894238 intron variant C/G 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: rs62056783
rs62056783
1 1.000 0.080 17 45897183 non coding transcript exon variant G/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs62055491
rs62055491
1 1.000 0.080 17 45873754 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs62054825
rs62054825
1 1.000 0.080 17 45852667 intron variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs62056781
rs62056781
1 1.000 0.080 17 45896533 non coding transcript exon variant T/C 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: rs62054820
rs62054820
1 1.000 0.080 17 45849389 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs916793
rs916793
2 1.000 0.080 17 45877320 intron variant G/A snv 0.14 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: rs56385754
rs56385754
1 1.000 0.080 17 45849889 intron variant G/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs62054822
rs62054822
1 1.000 0.080 17 45850342 intron variant A/G snv 0.16 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