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rs730881897

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
Position23637954
GenePALB2
is asnp
is mentioned by
dbSNPrs730881897
ebirs730881897
HLIrs730881897
Exacrs730881897
Varsomers730881897
Maprs730881897
PheGenIrs730881897
hapmaprs730881897
1000 genomesrs730881897
hgdprs730881897
ensemblrs730881897
gopubmedrs730881897
geneviewrs730881897
scholarrs730881897
googlers730881897
pharmgkbrs730881897
gwascentralrs730881897
openSNPrs730881897
23andMers730881897
23andMe allrs730881897
SNP Nexus

SNPshotrs730881897
SNPdbers730881897
MSV3drs730881897
GWAS Ctlgrs730881897
Max Magnitude7
ClinVar
Risk rs730881897(G;G)
Alt rs730881897(G;G)
Reference rs730881897(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PALB2
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23649275T>C
CLNSRC
CLNACC RCV000160858.2,