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rs152451

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 0 Benign, according to ClinVar
(G;G) 0 Benign, according to ClinVar
ReferenceGRCh38 38.1/142
Chromosome16
Position23634870
GenePALB2
is asnp
is mentioned by
dbSNPrs152451
ebirs152451
HLIrs152451
Exacrs152451
Varsomers152451
Maprs152451
PheGenIrs152451
hapmaprs152451
1000 genomesrs152451
hgdprs152451
ensemblrs152451
gopubmedrs152451
geneviewrs152451
scholarrs152451
googlers152451
pharmgkbrs152451
gwascentralrs152451
openSNPrs152451
23andMers152451
23andMe allrs152451
SNP Nexus

SNPshotrs152451
SNPdbers152451
MSV3drs152451
GWAS Ctlgrs152451
Max Magnitude0

[PMID 25636233OA-icon.png] Association of PALB2 sequence variants with the risk of familial and early-onset breast cancer in a South-American population


ClinVar
Risk rs152451(G;G)
Alt rs152451(G;G)
Reference rs152451(A;A)
Significance Other
Disease Familial cancer of breast not specified Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Familial cancer of breast not specified Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23646191T>C
CLNSRC Inc. PALB2 database
CLNACC RCV000114486.2, RCV000121747.2, RCV000128962.3,