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rs730881905

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 2-4 fold higher risk for breast cancer, depending on family history
(T;T) 7 Fanconi anemia, complementation group N
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23635858
GenePALB2
is asnp
is mentioned by
dbSNPrs730881905
ebirs730881905
HLIrs730881905
Exacrs730881905
Varsomers730881905
Maprs730881905
PheGenIrs730881905
hapmaprs730881905
1000 genomesrs730881905
hgdprs730881905
ensemblrs730881905
gopubmedrs730881905
geneviewrs730881905
scholarrs730881905
googlers730881905
pharmgkbrs730881905
gwascentralrs730881905
openSNPrs730881905
23andMers730881905
23andMe allrs730881905
SNP Nexus

SNPshotrs730881905
SNPdbers730881905
MSV3drs730881905
GWAS Ctlgrs730881905
Max Magnitude7
ClinVar
Risk rs730881905(T;T)
Alt rs730881905(T;T)
Reference rs730881905(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PALB2
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23647179C>A
CLNSRC
CLNACC RCV000160866.2,