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rs876659997

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs876659997(-;A)
Make rs876659997(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23629828
GenePALB2
is asnp
is mentioned by
dbSNPrs876659997
dbSNP (old)rs876659997
ClinGenrs876659997
ebirs876659997
HLIrs876659997
Exacrs876659997
Gnomadrs876659997
Varsomers876659997
Maprs876659997
PheGenIrs876659997
Biobankrs876659997
1000 genomesrs876659997
hgdprs876659997
ensemblrs876659997
gopubmedrs876659997
geneviewrs876659997
scholarrs876659997
googlers876659997
pharmgkbrs876659997
gwascentralrs876659997
openSNPrs876659997
23andMers876659997
23andMe allrs876659997
SNP Nexus

SNPshotrs876659997
SNPdbers876659997
MSV3drs876659997
GWAS Ctlgrs876659997
Max Magnitude0
ClinVar
Risk rs876659997(A;A)
Alt rs876659997(A;A)
Reference Rs876659997(-;-)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23641150dupT
CLNSRC
CLNACC RCV000218689.2, RCV000236131.2, RCV000468481.1,