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rs730881884

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
Position23641115
GeneDCTN5, PALB2
is asnp
is mentioned by
dbSNPrs730881884
dbSNP (old)rs730881884
ClinGenrs730881884
ebirs730881884
HLIrs730881884
Exacrs730881884
Gnomadrs730881884
Varsomers730881884
Maprs730881884
PheGenIrs730881884
Biobankrs730881884
1000 genomesrs730881884
hgdprs730881884
ensemblrs730881884
gopubmedrs730881884
geneviewrs730881884
scholarrs730881884
googlers730881884
pharmgkbrs730881884
gwascentralrs730881884
openSNPrs730881884
23andMers730881884
23andMe allrs730881884
SNP Nexus

SNPshotrs730881884
SNPdbers730881884
MSV3drs730881884
GWAS Ctlgrs730881884
Max Magnitude7
ClinVar
Risk Rs730881884(T;T)
Alt Rs730881884(T;T)
Reference Rs730881884(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PALB2 DCTN5
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23652436C>A
CLNSRC
CLNACC RCV000160835.1,