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rs786203382

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GCAGAGCTTCCT;GCAGAGCTTCCT) 0 common in clinvar
(GCAGAGCTTCCT;TCAGA) 3 2-4 fold higher risk for breast cancer, depending on family history
(TCAGA;TCAGA) 7 Fanconi anemia, complementation group N
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position23629255
GenePALB2
is asnp
is mentioned by
dbSNPrs786203382
ebirs786203382
HLIrs786203382
Exacrs786203382
Varsomers786203382
Maprs786203382
PheGenIrs786203382
hapmaprs786203382
1000 genomesrs786203382
hgdprs786203382
ensemblrs786203382
gopubmedrs786203382
geneviewrs786203382
scholarrs786203382
googlers786203382
pharmgkbrs786203382
gwascentralrs786203382
openSNPrs786203382
23andMers786203382
23andMe allrs786203382
SNP Nexus

SNPshotrs786203382
SNPdbers786203382
MSV3drs786203382
GWAS Ctlgrs786203382
Max Magnitude7
ClinVar
Risk rs786203382(TCAGA;TCAGA)
Alt rs786203382(TCAGA;TCAGA)
Reference rs786203382(GCAGAGCTTCCT;GCAGAGCTTCCT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23640576_23640587delAGGAAGCTCTGCinsTCTGA
CLNSRC
CLNACC RCV000166663.1,