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rs786203821

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;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
Position23635606
GenePALB2
is asnp
is mentioned by
dbSNPrs786203821
ebirs786203821
HLIrs786203821
Exacrs786203821
Varsomers786203821
Maprs786203821
PheGenIrs786203821
hapmaprs786203821
1000 genomesrs786203821
hgdprs786203821
ensemblrs786203821
gopubmedrs786203821
geneviewrs786203821
scholarrs786203821
googlers786203821
pharmgkbrs786203821
gwascentralrs786203821
openSNPrs786203821
23andMers786203821
23andMe allrs786203821
SNP Nexus

SNPshotrs786203821
SNPdbers786203821
MSV3drs786203821
GWAS Ctlgrs786203821
Max Magnitude7
ClinVar
Risk rs786203821(T;T)
Alt rs786203821(T;T)
Reference rs786203821(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23646927G>A
CLNSRC
CLNACC RCV000167296.1,