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rs180177103

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 increased risk of breast cancer
(T;T) 7 Fanconi anemia, complementation group N
ReferenceGRCh38 38.1/141
Chromosome16
Position23634913
GenePALB2
is asnp
is mentioned by
dbSNPrs180177103
ebirs180177103
HLIrs180177103
Exacrs180177103
Varsomers180177103
Maprs180177103
PheGenIrs180177103
hapmaprs180177103
1000 genomesrs180177103
hgdprs180177103
ensemblrs180177103
gopubmedrs180177103
geneviewrs180177103
scholarrs180177103
googlers180177103
pharmgkbrs180177103
gwascentralrs180177103
openSNPrs180177103
23andMers180177103
23andMe allrs180177103
SNP Nexus

SNPshotrs180177103
SNPdbers180177103
MSV3drs180177103
GWAS Ctlgrs180177103
Max Magnitude7
ClinVar
Risk rs180177103(T;T)
Alt rs180177103(T;T)
Reference rs180177103(G;G)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23646234C>A
CLNSRC PALB2 database
CLNACC RCV000114484.1, RCV000131237.2,


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