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rs786201773

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;CA) 3 2-4 fold higher risk for breast cancer, depending on family history
(CA;CA) 0 common in clinvar
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position23634898
GenePALB2
is asnp
is mentioned by
dbSNPrs786201773
ebirs786201773
HLIrs786201773
Exacrs786201773
Varsomers786201773
Maprs786201773
PheGenIrs786201773
hapmaprs786201773
1000 genomesrs786201773
hgdprs786201773
ensemblrs786201773
gopubmedrs786201773
geneviewrs786201773
scholarrs786201773
googlers786201773
pharmgkbrs786201773
gwascentralrs786201773
openSNPrs786201773
23andMers786201773
23andMe allrs786201773
SNP Nexus

SNPshotrs786201773
SNPdbers786201773
MSV3drs786201773
GWAS Ctlgrs786201773
Max Magnitude7
ClinVar
Risk rs786201773(;)
Alt rs786201773(;)
Reference rs786201773(CA;CA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23646219_23646220delTG
CLNSRC
CLNACC RCV000164237.1,