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rs786203399

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;TT) 3 2-4 fold higher risk for breast cancer, depending on family history
(TT;TT) 0 common in clinvar
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position23635460
GenePALB2
is asnp
is mentioned by
dbSNPrs786203399
ebirs786203399
HLIrs786203399
Exacrs786203399
Varsomers786203399
Maprs786203399
PheGenIrs786203399
hapmaprs786203399
1000 genomesrs786203399
hgdprs786203399
ensemblrs786203399
gopubmedrs786203399
geneviewrs786203399
scholarrs786203399
googlers786203399
pharmgkbrs786203399
gwascentralrs786203399
openSNPrs786203399
23andMers786203399
23andMe allrs786203399
SNP Nexus

SNPshotrs786203399
SNPdbers786203399
MSV3drs786203399
GWAS Ctlgrs786203399
Max Magnitude7
ClinVar
Risk rs786203399(;)
Alt rs786203399(;)
Reference rs786203399(TT;TT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23646781_23646782delAA
CLNSRC
CLNACC RCV000166687.1,