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rs281865160

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281865160(-;-)
Make rs281865160(-;A)
ReferenceGRCh38 38.1/141
Chromosome8
Position31150358
GeneWRN
is asnp
is mentioned by
dbSNPrs281865160
ebirs281865160
HLIrs281865160
Exacrs281865160
Varsomers281865160
Maprs281865160
PheGenIrs281865160
hapmaprs281865160
1000 genomesrs281865160
hgdprs281865160
ensemblrs281865160
gopubmedrs281865160
geneviewrs281865160
scholarrs281865160
googlers281865160
pharmgkbrs281865160
gwascentralrs281865160
openSNPrs281865160
23andMers281865160
23andMe allrs281865160
SNP Nexus

SNPshotrs281865160
SNPdbers281865160
MSV3drs281865160
GWAS Ctlgrs281865160
Max Magnitude0
ClinVar
Risk rs281865160(;)
Alt rs281865160(;)
Reference rs281865160(A;A)
Significance Pathogenic
Disease Werner syndrome
Variation info
Gene WRN
CLNDBN Werner syndrome
Reversed 0
HGVS NC_000008.10:g.31007874delA
CLNSRC ClinVar GeneReviews
CLNACC RCV000032139.1,


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