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rs786202439

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 38.2/146
Chromosome16
Position23630224
GenePALB2
is asnp
is mentioned by
dbSNPrs786202439
ebirs786202439
HLIrs786202439
Exacrs786202439
Varsomers786202439
Maprs786202439
PheGenIrs786202439
hapmaprs786202439
1000 genomesrs786202439
hgdprs786202439
ensemblrs786202439
gopubmedrs786202439
geneviewrs786202439
scholarrs786202439
googlers786202439
pharmgkbrs786202439
gwascentralrs786202439
openSNPrs786202439
23andMers786202439
23andMe allrs786202439
SNP Nexus

SNPshotrs786202439
SNPdbers786202439
MSV3drs786202439
GWAS Ctlgrs786202439
Max Magnitude7
ClinVar
Risk rs786202439(T;T)
Alt rs786202439(T;T)
Reference rs786202439(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.23641545C>A
CLNSRC
CLNACC RCV000165251.1,