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

rs869312772

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312772(-;-)
Make rs869312772(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23635383
GenePALB2
is asnp
is mentioned by
dbSNPrs869312772
ebirs869312772
HLIrs869312772
Exacrs869312772
Varsomers869312772
Maprs869312772
PheGenIrs869312772
hapmaprs869312772
1000 genomesrs869312772
hgdprs869312772
ensemblrs869312772
gopubmedrs869312772
geneviewrs869312772
scholarrs869312772
googlers869312772
pharmgkbrs869312772
gwascentralrs869312772
openSNPrs869312772
23andMers869312772
23andMe allrs869312772
SNP Nexus

SNPshotrs869312772
SNPdbers869312772
MSV3drs869312772
GWAS Ctlgrs869312772
Max Magnitude0
ClinVar
Risk rs869312772(;)
Alt rs869312772(;)
Reference rs869312772(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23646704delG
CLNSRC
CLNACC RCV000210113.1,