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

rs876658136

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs876658136(-;-)
Make rs876658136(-;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23607967
GenePALB2
is asnp
is mentioned by
dbSNPrs876658136
dbSNP (old)rs876658136
ClinGenrs876658136
ebirs876658136
HLIrs876658136
Exacrs876658136
Gnomadrs876658136
Varsomers876658136
Maprs876658136
PheGenIrs876658136
Biobankrs876658136
1000 genomesrs876658136
hgdprs876658136
ensemblrs876658136
gopubmedrs876658136
geneviewrs876658136
scholarrs876658136
googlers876658136
pharmgkbrs876658136
gwascentralrs876658136
openSNPrs876658136
23andMers876658136
23andMe allrs876658136
SNP Nexus

SNPshotrs876658136
SNPdbers876658136
MSV3drs876658136
GWAS Ctlgrs876658136
Max Magnitude0
ClinVar
Risk rs876658136(-;-)
Alt rs876658136(-;-)
Reference Rs876658136(TG;TG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23619288_23619289delCA
CLNSRC
CLNACC RCV000215931.1,