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rs730881866

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;C) 3 2-4 fold higher risk for breast cancer, depending on family history
(C;C) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23630122
GenePALB2
is asnp
is mentioned by
dbSNPrs730881866
ebirs730881866
HLIrs730881866
Exacrs730881866
Varsomers730881866
Maprs730881866
PheGenIrs730881866
hapmaprs730881866
1000 genomesrs730881866
hgdprs730881866
ensemblrs730881866
gopubmedrs730881866
geneviewrs730881866
scholarrs730881866
googlers730881866
pharmgkbrs730881866
gwascentralrs730881866
openSNPrs730881866
23andMers730881866
23andMe allrs730881866
SNP Nexus

SNPshotrs730881866
SNPdbers730881866
MSV3drs730881866
GWAS Ctlgrs730881866
Max Magnitude7
ClinVar
Risk rs730881866(;)
Alt rs730881866(;)
Reference rs730881866(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000016.9:g.23641443delG
CLNSRC
CLNACC RCV000160807.1, RCV000220938.1,