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rs753153576

From SNPedia

Orientationplus
Stabilizedplus
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 38.2/144
Chromosome16
Position23626235
GenePALB2
is asnp
is mentioned by
dbSNPrs753153576
dbSNP (old)rs753153576
ClinGenrs753153576
ebirs753153576
HLIrs753153576
Exacrs753153576
Varsomers753153576
Maprs753153576
PheGenIrs753153576
Biobankrs753153576
1000 genomesrs753153576
hgdprs753153576
ensemblrs753153576
gopubmedrs753153576
geneviewrs753153576
scholarrs753153576
googlers753153576
pharmgkbrs753153576
gwascentralrs753153576
openSNPrs753153576
23andMers753153576
23andMe allrs753153576
SNP Nexus

SNPshotrs753153576
SNPdbers753153576
MSV3drs753153576
GWAS Ctlgrs753153576
Merged fromRs786202646
Max Magnitude7
ClinVar
Risk rs753153576(A;A) rs753153576(G;G) Rs753153576(T;T)
Alt rs753153576(A;A) rs753153576(G;G) Rs753153576(T;T)
Reference Rs753153576(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Reversed 0
HGVS NC_000016.9:g.23637556C>A; NC_000016.9:g.23637556C>G
CLNSRC
CLNACC RCV000165555.3, RCV000487378.1, RCV000409294.1,