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rs730881867

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;G) 3 2-4 fold higher risk for breast cancer, depending on family history
(G;G) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23630000
GenePALB2
is asnp
is mentioned by
dbSNPrs730881867
ebirs730881867
HLIrs730881867
Exacrs730881867
Varsomers730881867
Maprs730881867
PheGenIrs730881867
hapmaprs730881867
1000 genomesrs730881867
hgdprs730881867
ensemblrs730881867
gopubmedrs730881867
geneviewrs730881867
scholarrs730881867
googlers730881867
pharmgkbrs730881867
gwascentralrs730881867
openSNPrs730881867
23andMers730881867
23andMe allrs730881867
SNP Nexus

SNPshotrs730881867
SNPdbers730881867
MSV3drs730881867
GWAS Ctlgrs730881867
Max Magnitude7
ClinVar
Risk rs730881867(;)
Alt rs730881867(;)
Reference rs730881867(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23641321delC
CLNSRC
CLNACC RCV000160808.1,