Have questions? Visit https://www.reddit.com/r/SNPedia

rs876658813

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658813(-;-)
Make rs876658813(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23629666
GenePALB2
is asnp
is mentioned by
dbSNPrs876658813
ClinGenrs876658813
ebirs876658813
HLIrs876658813
Exacrs876658813
Varsomers876658813
Maprs876658813
PheGenIrs876658813
hapmaprs876658813
1000 genomesrs876658813
hgdprs876658813
ensemblrs876658813
gopubmedrs876658813
geneviewrs876658813
scholarrs876658813
googlers876658813
pharmgkbrs876658813
gwascentralrs876658813
openSNPrs876658813
23andMers876658813
23andMe allrs876658813
SNP Nexus

SNPshotrs876658813
SNPdbers876658813
MSV3drs876658813
GWAS Ctlgrs876658813
Max Magnitude0
ClinVar
Risk rs876658813(-;-)
Alt rs876658813(-;-)
Reference Rs876658813(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000016.9:g.23640987delC
CLNSRC
CLNACC RCV000217161.1, RCV000478191.1,