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rs587776419

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 significantly increased risk of breast cancer
(T;T) 7 Fanconi anemia, complementation group N
ReferenceGRCh38 38.1/142
Chromosome16
Position23624008
GenePALB2
is asnp
is mentioned by
dbSNPrs587776419
ebirs587776419
HLIrs587776419
Exacrs587776419
Varsomers587776419
Maprs587776419
PheGenIrs587776419
hapmaprs587776419
1000 genomesrs587776419
hgdprs587776419
ensemblrs587776419
gopubmedrs587776419
geneviewrs587776419
scholarrs587776419
googlers587776419
pharmgkbrs587776419
gwascentralrs587776419
openSNPrs587776419
23andMers587776419
23andMe allrs587776419
SNP Nexus

SNPshotrs587776419
SNPdbers587776419
MSV3drs587776419
GWAS Ctlgrs587776419
Max Magnitude7
ClinVar
Risk rs587776419(A,T;A,T)
Alt rs587776419(A,T;A,T)
Reference rs587776419(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PALB2
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23635329C>A; NC_000016.9:g.23635329C>T
CLNSRC ClinVar
CLNACC RCV000133481.1, RCV000160847.1,