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rs876658773

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 5 PALB2-related cancer risk
Make rs876658773(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23603662
GenePALB2
is asnp
is mentioned by
dbSNPrs876658773
dbSNP (classic)rs876658773
ClinGenrs876658773
ebirs876658773
HLIrs876658773
Exacrs876658773
Gnomadrs876658773
Varsomers876658773
LitVarrs876658773
Maprs876658773
PheGenIrs876658773
Biobankrs876658773
1000 genomesrs876658773
hgdprs876658773
ensemblrs876658773
geneviewrs876658773
scholarrs876658773
googlers876658773
pharmgkbrs876658773
gwascentralrs876658773
openSNPrs876658773
23andMers876658773
SNPshotrs876658773
SNPdbers876658773
MSV3drs876658773
GWAS Ctlgrs876658773
Max Magnitude5
ClinVar
Risk rs876658773(T;T)
Alt rs876658773(T;T)
Reference Rs876658773(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23614983C>A
CLNSRC
CLNACC RCV000215626.1,