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rs180177138

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;G) 3 increased risk of breast cancer
(G;G) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome16
Position23603523
GenePALB2
is asnp
is mentioned by
dbSNPrs180177138
ebirs180177138
HLIrs180177138
Exacrs180177138
Varsomers180177138
Maprs180177138
PheGenIrs180177138
hapmaprs180177138
1000 genomesrs180177138
hgdprs180177138
ensemblrs180177138
gopubmedrs180177138
geneviewrs180177138
scholarrs180177138
googlers180177138
pharmgkbrs180177138
gwascentralrs180177138
openSNPrs180177138
23andMers180177138
23andMe allrs180177138
SNP Nexus

SNPshotrs180177138
SNPdbers180177138
MSV3drs180177138
GWAS Ctlgrs180177138
Max Magnitude7
ClinVar
Risk rs180177138(;)
Alt rs180177138(;)
Reference rs180177138(G;G)
Significance Pathogenic
Disease Familial cancer of breast Pancreatic cancer 3
Variation info
Gene PALB2
CLNDBN Familial cancer of breast Pancreatic cancer 3
Reversed 1
HGVS NC_000016.9:g.23614844delC
CLNSRC PALB2 database
CLNACC RCV000114631.1, RCV000114632.1,


[PMID 21184274] PALB2 germline mutations in familial breast cancer cases with personal and family history of pancreatic cancer.