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rs587782050

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 7 Fanconi anemia, complementation group N
(A;G) 3 2-4 fold higher risk for breast cancer, depending on family history
(G;G) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23603544
GenePALB2
is asnp
is mentioned by
dbSNPrs587782050
ebirs587782050
HLIrs587782050
Exacrs587782050
Varsomers587782050
Maprs587782050
PheGenIrs587782050
hapmaprs587782050
1000 genomesrs587782050
hgdprs587782050
ensemblrs587782050
gopubmedrs587782050
geneviewrs587782050
scholarrs587782050
googlers587782050
pharmgkbrs587782050
gwascentralrs587782050
openSNPrs587782050
23andMers587782050
23andMe allrs587782050
SNP Nexus

SNPshotrs587782050
SNPdbers587782050
MSV3drs587782050
GWAS Ctlgrs587782050
Max Magnitude7
ClinVar
Risk rs587782050(A;A)
Alt rs587782050(A;A)
Reference rs587782050(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23614865C>T
CLNSRC
CLNACC RCV000130518.2,