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rs587776417

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common/normal
(G;T) 3 significantly increased risk of breast cancer
(T;T) 7 Fanconi anemia, complementation group N
ReferenceGRCh38 38.1/142
Chromosome16
Position23629276
GenePALB2
is asnp
is mentioned by
dbSNPrs587776417
ebirs587776417
HLIrs587776417
Exacrs587776417
Varsomers587776417
Maprs587776417
PheGenIrs587776417
hapmaprs587776417
1000 genomesrs587776417
hgdprs587776417
ensemblrs587776417
gopubmedrs587776417
geneviewrs587776417
scholarrs587776417
googlers587776417
pharmgkbrs587776417
gwascentralrs587776417
openSNPrs587776417
23andMers587776417
23andMe allrs587776417
SNP Nexus

SNPshotrs587776417
SNPdbers587776417
MSV3drs587776417
GWAS Ctlgrs587776417
Max Magnitude7
ClinVar
Risk rs587776417(C,T;C,T)
Alt rs587776417(C,T;C,T)
Reference rs587776417(G;G)
Significance Other
Disease Pancreatic cancer 3 Familial cancer of breast not provided
Variation info
Gene PALB2
CLNDBN Pancreatic cancer 3 Familial cancer of breast not provided
Reversed 1
HGVS NC_000016.9:g.23640597C>A; NC_000016.9:g.23640597C>G
CLNSRC OMIM Allelic Variant PALB2 database
CLNACC RCV000001312.2, RCV000114532.1, RCV000133479.1, RCV000198016.1,