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rs786203892

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;AGGTAA) 3 2-4 fold higher risk for breast cancer, depending on family history
(AGGTAA;AGGTAA) 0 common in clinvar
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position23626232
GenePALB2
is asnp
is mentioned by
dbSNPrs786203892
ebirs786203892
HLIrs786203892
Exacrs786203892
Varsomers786203892
Maprs786203892
PheGenIrs786203892
hapmaprs786203892
1000 genomesrs786203892
hgdprs786203892
ensemblrs786203892
gopubmedrs786203892
geneviewrs786203892
scholarrs786203892
googlers786203892
pharmgkbrs786203892
gwascentralrs786203892
openSNPrs786203892
23andMers786203892
23andMe allrs786203892
SNP Nexus

SNPshotrs786203892
SNPdbers786203892
MSV3drs786203892
GWAS Ctlgrs786203892
Max Magnitude7
ClinVar
Risk rs786203892(;)
Alt rs786203892(;)
Reference rs786203892(AGGTAA;AGGTAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23637553_23637558delTTACCT
CLNSRC
CLNACC RCV000167394.1,