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rs587781480

From SNPedia

Orientationplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs587781480(CTTTGTGGTAAGTTT;CTTTGTGGTAAGTTT)
Make rs587781480(CTTTGTGGTAAGTTT;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32341191
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587781480
ebirs587781480
HLIrs587781480
Exacrs587781480
Varsomers587781480
Maprs587781480
PheGenIrs587781480
hapmaprs587781480
1000 genomesrs587781480
hgdprs587781480
ensemblrs587781480
gopubmedrs587781480
geneviewrs587781480
scholarrs587781480
googlers587781480
pharmgkbrs587781480
gwascentralrs587781480
openSNPrs587781480
23andMers587781480
23andMe allrs587781480
SNP Nexus

SNPshotrs587781480
SNPdbers587781480
MSV3drs587781480
GWAS Ctlgrs587781480
Max Magnitude0
ClinVar
Risk rs587781480(CTTTGTGGTAAGTTT;CTTTGTGGTAAGTTT)
Alt rs587781480(CTTTGTGGTAAGTTT;CTTTGTGGTAAGTTT)
Reference rs587781480(TA;TA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32915328_32915329delTAinsCTTTGTGGTAAGTTT
CLNSRC
CLNACC RCV000129434.2,