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rs3087425

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3087425(C;T)
Make rs3087425(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position31120294
GeneWRN
is asnp
is mentioned by
dbSNPrs3087425
ebirs3087425
HLIrs3087425
Exacrs3087425
Varsomers3087425
Maprs3087425
PheGenIrs3087425
hapmaprs3087425
1000 genomesrs3087425
hgdprs3087425
ensemblrs3087425
gopubmedrs3087425
geneviewrs3087425
scholarrs3087425
googlers3087425
pharmgkbrs3087425
gwascentralrs3087425
openSNPrs3087425
23andMers3087425
23andMe allrs3087425
SNP Nexus

SNPshotrs3087425
SNPdbers3087425
MSV3drs3087425
GWAS Ctlgrs3087425
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 26690424] Association of the rs1346044 Polymorphism of the Werner Syndrome Gene RECQL2 with Increased Risk and Premature Onset of Breast Cancer.

ClinVar
Risk rs3087425(T;T)
Alt rs3087425(T;T)
Reference rs3087425(C;C)
Significance Other
Disease Werner syndrome not specified
Variation info
Gene WRN
CLNDBN Werner syndrome not specified
Reversed 0
HGVS NC_000008.10:g.30977810C>T
CLNSRC
CLNACC RCV000032137.1, RCV000122280.2,