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rs587776426

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0 common/normal
(-;A) 3 2-4 fold higher risk for breast cancer, depending on family history
(A;A) 7 Fanconi anemia, complementation group N
ReferenceGRCh38 38.1/142
Chromosome16
Position23603563
GenePALB2
is asnp
is mentioned by
dbSNPrs587776426
ebirs587776426
HLIrs587776426
Exacrs587776426
Varsomers587776426
Maprs587776426
PheGenIrs587776426
hapmaprs587776426
1000 genomesrs587776426
hgdprs587776426
ensemblrs587776426
gopubmedrs587776426
geneviewrs587776426
scholarrs587776426
googlers587776426
pharmgkbrs587776426
gwascentralrs587776426
openSNPrs587776426
23andMers587776426
23andMe allrs587776426
SNP Nexus

SNPshotrs587776426
SNPdbers587776426
MSV3drs587776426
GWAS Ctlgrs587776426
Max Magnitude7
ClinVar
Risk rs587776426(A;A)
Alt rs587776426(A;A)
Reference rs587776426(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome not provided Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000016.9:g.23614885dupT
CLNSRC ClinVar GeneDx
CLNACC RCV000116106.2, RCV000133488.1, RCV000200796.2, RCV000214210.1,