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rs281865158

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs281865158(-;-)
Make rs281865158(-;T)
Make rs281865158(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position31111705
GeneWRN
is asnp
is mentioned by
dbSNPrs281865158
ebirs281865158
HLIrs281865158
Exacrs281865158
Varsomers281865158
Maprs281865158
PheGenIrs281865158
hapmaprs281865158
1000 genomesrs281865158
hgdprs281865158
ensemblrs281865158
gopubmedrs281865158
geneviewrs281865158
scholarrs281865158
googlers281865158
pharmgkbrs281865158
gwascentralrs281865158
openSNPrs281865158
23andMers281865158
23andMe allrs281865158
SNP Nexus

SNPshotrs281865158
SNPdbers281865158
MSV3drs281865158
GWAS Ctlgrs281865158
Max Magnitude0
ClinVar
Risk rs281865158(T;T)
Alt rs281865158(T;T)
Reference rs281865158(;)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.30969221dupT
CLNSRC ClinVar GeneReviews
CLNACC RCV000032136.1,


[PMID 16673358OA-icon.png] The spectrum of WRN mutations in Werner syndrome patients.


[PMID 20443122] WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.