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rs45551636

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 1 Likely to be a benign polymorphism, according to ClinVar
(A;G) 1 Likely to be a benign polymorphism, according to ClinVar
(G;G) 0 common in clinvar
ReferenceGRCh38 38.1/142
Chromosome16
Position23622972
GenePALB2
is asnp
is mentioned by
dbSNPrs45551636
ebirs45551636
HLIrs45551636
Exacrs45551636
Varsomers45551636
Maprs45551636
PheGenIrs45551636
hapmaprs45551636
1000 genomesrs45551636
hgdprs45551636
ensemblrs45551636
gopubmedrs45551636
geneviewrs45551636
scholarrs45551636
googlers45551636
pharmgkbrs45551636
gwascentralrs45551636
openSNPrs45551636
23andMers45551636
23andMe allrs45551636
SNP Nexus

SNPshotrs45551636
SNPdbers45551636
MSV3drs45551636
GWAS Ctlgrs45551636
Max Magnitude1

[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 rs45551636(A;A)
Alt rs45551636(A;A)
Reference rs45551636(G;G)
Significance Other
Disease Familial cancer of breast Pancreatic cancer 3 not specified Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Familial cancer of breast Pancreatic cancer 3 not specified Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23634293C>T
CLNSRC PALB2 database
CLNACC RCV000114578.6, RCV000114579.1, RCV000121762.1, RCV000127300.5,