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rs878855122

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855122(G;T)
Make rs878855122(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23638099
GenePALB2
is asnp
is mentioned by
dbSNPrs878855122
ebirs878855122
HLIrs878855122
Exacrs878855122
Varsomers878855122
Maprs878855122
PheGenIrs878855122
hapmaprs878855122
1000 genomesrs878855122
hgdprs878855122
ensemblrs878855122
gopubmedrs878855122
geneviewrs878855122
scholarrs878855122
googlers878855122
pharmgkbrs878855122
gwascentralrs878855122
openSNPrs878855122
23andMers878855122
23andMe allrs878855122
SNP Nexus

SNPshotrs878855122
SNPdbers878855122
MSV3drs878855122
GWAS Ctlgrs878855122
Max Magnitude0
ClinVar
Risk rs878855122(T;T)
Alt rs878855122(T;T)
Reference rs878855122(G;G)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23649420C>A
CLNSRC
CLNACC RCV000228882.1,