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rs587776407

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 significantly increased risk of breast cancer
ReferenceGRCh38 38.1/142
Chromosome16
Position23636095
GenePALB2
is asnp
is mentioned by
dbSNPrs587776407
ebirs587776407
HLIrs587776407
Exacrs587776407
Varsomers587776407
Maprs587776407
PheGenIrs587776407
hapmaprs587776407
1000 genomesrs587776407
hgdprs587776407
ensemblrs587776407
gopubmedrs587776407
geneviewrs587776407
scholarrs587776407
googlers587776407
pharmgkbrs587776407
gwascentralrs587776407
openSNPrs587776407
23andMers587776407
23andMe allrs587776407
SNP Nexus

SNPshotrs587776407
SNPdbers587776407
MSV3drs587776407
GWAS Ctlgrs587776407
Max Magnitude3
ClinVar
Risk rs587776407(T;T)
Alt rs587776407(T;T)
Reference rs587776407(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PALB2
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23647416G>A
CLNSRC ClinVar
CLNACC RCV000133491.1,