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rs786203245

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;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
Position23638131
GenePALB2
is asnp
is mentioned by
dbSNPrs786203245
ebirs786203245
HLIrs786203245
Exacrs786203245
Varsomers786203245
Maprs786203245
PheGenIrs786203245
hapmaprs786203245
1000 genomesrs786203245
hgdprs786203245
ensemblrs786203245
gopubmedrs786203245
geneviewrs786203245
scholarrs786203245
googlers786203245
pharmgkbrs786203245
gwascentralrs786203245
openSNPrs786203245
23andMers786203245
23andMe allrs786203245
SNP Nexus

SNPshotrs786203245
SNPdbers786203245
MSV3drs786203245
GWAS Ctlgrs786203245
Max Magnitude7
ClinVar
Risk rs786203245(T;T)
Alt rs786203245(T;T)
Reference rs786203245(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23649452T>A
CLNSRC
CLNACC RCV000166471.1, RCV000198571.1,