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rs45476495

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45476495(A;A)
Make rs45476495(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23626310
GenePALB2
is asnp
is mentioned by
dbSNPrs45476495
ebirs45476495
HLIrs45476495
Exacrs45476495
Varsomers45476495
Maprs45476495
PheGenIrs45476495
hapmaprs45476495
1000 genomesrs45476495
hgdprs45476495
ensemblrs45476495
gopubmedrs45476495
geneviewrs45476495
scholarrs45476495
googlers45476495
pharmgkbrs45476495
gwascentralrs45476495
openSNPrs45476495
23andMers45476495
23andMe allrs45476495
SNP Nexus

SNPshotrs45476495
SNPdbers45476495
MSV3drs45476495
GWAS Ctlgrs45476495
Max Magnitude0
ClinVar
Risk rs45476495(A;A)
Alt rs45476495(A;A)
Reference rs45476495(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23637631C>A; NC_000016.9:g.23637631C>T
CLNSRC PALB2 database
CLNACC RCV000217992.1, RCV000114549.4, RCV000131257.2,