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rs587780206

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
(CA;TG) 3 2-4 fold higher risk for breast cancer, depending on family history
(TG;TG) 7 Fanconi anemia, complementation group N
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23634870
GenePALB2
is asnp
is mentioned by
dbSNPrs587780206
ebirs587780206
HLIrs587780206
Exacrs587780206
Varsomers587780206
Maprs587780206
PheGenIrs587780206
hapmaprs587780206
1000 genomesrs587780206
hgdprs587780206
ensemblrs587780206
gopubmedrs587780206
geneviewrs587780206
scholarrs587780206
googlers587780206
pharmgkbrs587780206
gwascentralrs587780206
openSNPrs587780206
23andMers587780206
23andMe allrs587780206
SNP Nexus

SNPshotrs587780206
SNPdbers587780206
MSV3drs587780206
GWAS Ctlgrs587780206
Max Magnitude7
ClinVar
Risk rs587780206(TG;TG)
Alt rs587780206(TG;TG)
Reference rs587780206(CA;CA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000016.9:g.23646191_23646192delTGinsCA
CLNSRC
CLNACC RCV000116070.4, RCV000235193.1,