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rs730881872

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;A) 3 2-4 fold higher risk for breast cancer, depending on family history
(A;A) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23635487
GenePALB2
is asnp
is mentioned by
dbSNPrs730881872
ebirs730881872
HLIrs730881872
Exacrs730881872
Varsomers730881872
Maprs730881872
PheGenIrs730881872
hapmaprs730881872
1000 genomesrs730881872
hgdprs730881872
ensemblrs730881872
gopubmedrs730881872
geneviewrs730881872
scholarrs730881872
googlers730881872
pharmgkbrs730881872
gwascentralrs730881872
openSNPrs730881872
23andMers730881872
23andMe allrs730881872
SNP Nexus

SNPshotrs730881872
SNPdbers730881872
MSV3drs730881872
GWAS Ctlgrs730881872
Max Magnitude7
ClinVar
Risk rs730881872(;)
Alt rs730881872(;)
Reference rs730881872(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23646808delT
CLNSRC
CLNACC RCV000160814.1, RCV000230419.1,