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rs786203346

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
(-;TT) 3 2-4 fold higher risk for breast cancer, depending on family history
(TT;TT) 7 Fanconi anemia, complementation group N


Make rs786203346(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position23634928
GenePALB2
is asnp
is mentioned by
dbSNPrs786203346
ebirs786203346
HLIrs786203346
Exacrs786203346
Varsomers786203346
Maprs786203346
PheGenIrs786203346
hapmaprs786203346
1000 genomesrs786203346
hgdprs786203346
ensemblrs786203346
gopubmedrs786203346
geneviewrs786203346
scholarrs786203346
googlers786203346
pharmgkbrs786203346
gwascentralrs786203346
openSNPrs786203346
23andMers786203346
23andMe allrs786203346
SNP Nexus

SNPshotrs786203346
SNPdbers786203346
MSV3drs786203346
GWAS Ctlgrs786203346
Max Magnitude7
ClinVar
Risk Rs786203346(TT;TT)
Alt Rs786203346(TT;TT)
Reference Rs786203346(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23646250_23646251dupAA
CLNSRC
CLNACC RCV000166617.2,