Have questions? Visit https://www.reddit.com/r/SNPedia

rs786203775

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
Position23622979
GenePALB2
is asnp
is mentioned by
dbSNPrs786203775
ebirs786203775
HLIrs786203775
Exacrs786203775
Varsomers786203775
Maprs786203775
PheGenIrs786203775
hapmaprs786203775
1000 genomesrs786203775
hgdprs786203775
ensemblrs786203775
gopubmedrs786203775
geneviewrs786203775
scholarrs786203775
googlers786203775
pharmgkbrs786203775
gwascentralrs786203775
openSNPrs786203775
23andMers786203775
23andMe allrs786203775
SNP Nexus

SNPshotrs786203775
SNPdbers786203775
MSV3drs786203775
GWAS Ctlgrs786203775
Max Magnitude7
ClinVar
Risk rs786203775(T;T)
Alt rs786203775(T;T)
Reference rs786203775(G;G)
Significance 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.23634300C>A
CLNSRC
CLNACC RCV000167226.1, RCV000227242.1,