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rs587776413

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 3 significantly increased risk of breast cancer
(G;G) 7 Fanconi anemia, complementation group N
ReferenceGRCh38 38.1/142
Chromosome16
Position23634975
GenePALB2
is asnp
is mentioned by
dbSNPrs587776413
ebirs587776413
HLIrs587776413
Exacrs587776413
Varsomers587776413
Maprs587776413
PheGenIrs587776413
hapmaprs587776413
1000 genomesrs587776413
hgdprs587776413
ensemblrs587776413
gopubmedrs587776413
geneviewrs587776413
scholarrs587776413
googlers587776413
pharmgkbrs587776413
gwascentralrs587776413
openSNPrs587776413
23andMers587776413
23andMe allrs587776413
SNP Nexus

SNPshotrs587776413
SNPdbers587776413
MSV3drs587776413
GWAS Ctlgrs587776413
Max Magnitude7
ClinVar
Risk rs587776413(G;G)
Alt rs587776413(G;G)
Reference rs587776413(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PALB2
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23646296G>C
CLNSRC ClinVar
CLNACC RCV000133475.1,