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rs730881879

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 3 2-4 fold higher risk for breast cancer, depending on family history
(G;G) 7 Fanconi anemia, complementation group N
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23636336
GenePALB2
is asnp
is mentioned by
dbSNPrs730881879
ebirs730881879
HLIrs730881879
Exacrs730881879
Varsomers730881879
Maprs730881879
PheGenIrs730881879
hapmaprs730881879
1000 genomesrs730881879
hgdprs730881879
ensemblrs730881879
gopubmedrs730881879
geneviewrs730881879
scholarrs730881879
googlers730881879
pharmgkbrs730881879
gwascentralrs730881879
openSNPrs730881879
23andMers730881879
23andMe allrs730881879
SNP Nexus

SNPshotrs730881879
SNPdbers730881879
MSV3drs730881879
GWAS Ctlgrs730881879
Max Magnitude7
ClinVar
Risk rs730881879(G;G)
Alt rs730881879(G;G)
Reference rs730881879(A;A)
Significance Pathogenic
Disease not provided Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PALB2
CLNDBN not provided Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000016.9:g.23647657T>C
CLNSRC
CLNACC RCV000160830.2, RCV000206312.2, RCV000213220.1,