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rs180177124

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 increased risk of breast cancer
(T;T) 7 Fanconi anemia, complementation group N
ReferenceGRCh38 38.1/141
Chromosome16
Position23624082
GenePALB2
is asnp
is mentioned by
dbSNPrs180177124
ebirs180177124
HLIrs180177124
Exacrs180177124
Varsomers180177124
Maprs180177124
PheGenIrs180177124
hapmaprs180177124
1000 genomesrs180177124
hgdprs180177124
ensemblrs180177124
gopubmedrs180177124
geneviewrs180177124
scholarrs180177124
googlers180177124
pharmgkbrs180177124
gwascentralrs180177124
openSNPrs180177124
23andMers180177124
23andMe allrs180177124
SNP Nexus

SNPshotrs180177124
SNPdbers180177124
MSV3drs180177124
GWAS Ctlgrs180177124
Max Magnitude7
ClinVar
Risk rs180177124(T;T)
Alt rs180177124(T;T)
Reference rs180177124(C;C)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23635403G>A
CLNSRC PALB2 database
CLNACC RCV000114557.1,


[PMID 21165770OA-icon.png] PALB2 mutations in German and Russian patients with bilateral breast cancer.