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rs587782217

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782217(G;T)
Make rs587782217(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23603528
GenePALB2
is asnp
is mentioned by
dbSNPrs587782217
ebirs587782217
HLIrs587782217
Exacrs587782217
Varsomers587782217
Maprs587782217
PheGenIrs587782217
hapmaprs587782217
1000 genomesrs587782217
hgdprs587782217
ensemblrs587782217
gopubmedrs587782217
geneviewrs587782217
scholarrs587782217
googlers587782217
pharmgkbrs587782217
gwascentralrs587782217
openSNPrs587782217
23andMers587782217
23andMe allrs587782217
SNP Nexus

SNPshotrs587782217
SNPdbers587782217
MSV3drs587782217
GWAS Ctlgrs587782217
Max Magnitude0
ClinVar
Risk rs587782217(T;T)
Alt rs587782217(T;T)
Reference rs587782217(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.23614849C>A; NC_000016.9:g.23614849C>T
CLNSRC
CLNACC RCV000130901.2, RCV000235984.1,