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rs878855099

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855099(G;T)
Make rs878855099(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23635177
GenePALB2
is asnp
is mentioned by
dbSNPrs878855099
ClinGenrs878855099
ebirs878855099
HLIrs878855099
Exacrs878855099
Varsomers878855099
Maprs878855099
PheGenIrs878855099
hapmaprs878855099
1000 genomesrs878855099
hgdprs878855099
ensemblrs878855099
gopubmedrs878855099
geneviewrs878855099
scholarrs878855099
googlers878855099
pharmgkbrs878855099
gwascentralrs878855099
openSNPrs878855099
23andMers878855099
23andMe allrs878855099
SNP Nexus

SNPshotrs878855099
SNPdbers878855099
MSV3drs878855099
GWAS Ctlgrs878855099
Max Magnitude0
ClinVar
Risk rs878855099(T;T)
Alt rs878855099(T;T)
Reference Rs878855099(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.23646498C>A
CLNSRC
CLNACC RCV000231944.1,