rs17847577
From SNPedia
Werner's Syndrome |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | normal |
(C;T) | 5 | Unaffected carrier for Werner's Syndrome |
(T;T) | 7.5 | Werner's Syndrome |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 31081132 |
Gene | WRN |
is a | snp |
is | mentioned by |
dbSNP | rs17847577 |
dbSNP (classic) | rs17847577 |
ClinGen | rs17847577 |
ebi | rs17847577 |
HLI | rs17847577 |
Exac | rs17847577 |
Gnomad | rs17847577 |
Varsome | rs17847577 |
LitVar | rs17847577 |
Map | rs17847577 |
PheGenI | rs17847577 |
Biobank | rs17847577 |
1000 genomes | rs17847577 |
hgdp | rs17847577 |
ensembl | rs17847577 |
geneview | rs17847577 |
scholar | rs17847577 |
rs17847577 | |
pharmgkb | rs17847577 |
gwascentral | rs17847577 |
openSNP | rs17847577 |
23andMe | rs17847577 |
SNPshot | rs17847577 |
SNPdbe | rs17847577 |
MSV3d | rs17847577 |
GWAS Ctlg | rs17847577 |
Max Magnitude | 7.5 |
rs17847577, also known as R368X, Arg368Ter, Arg369Ter, c.1105C>T or 1336C>T) represents the most common WRN mutation seen in Caucasians as well as all other non-Japanese populations, perhaps representing ~20% of all Werner Syndrome cases.
ClinVar | |
---|---|
Risk | Rs17847577(T;T) |
Alt | Rs17847577(T;T) |
Reference | Rs17847577(C;C) |
Significance | Pathogenic |
Disease | Werner syndrome |
Variation | info |
Gene | WRN |
CLNDBN | Werner syndrome |
Reversed | 0 |
HGVS | NC_000008.10:g.30938648C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000005782.4, |
[PMID 16673358] The spectrum of WRN mutations in Werner syndrome patients.