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rs587782799

From SNPedia

Orientationplus
Geno Mag Summary
(AGTT;AGTT) 0 common in clinvar
Make rs587782799(-;-)
Make rs587782799(-;GTTA)
Make rs587782799(GTTA;GTTA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32340581
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782799
ebirs587782799
HLIrs587782799
Exacrs587782799
Varsomers587782799
Maprs587782799
PheGenIrs587782799
hapmaprs587782799
1000 genomesrs587782799
hgdprs587782799
ensemblrs587782799
gopubmedrs587782799
geneviewrs587782799
scholarrs587782799
googlers587782799
pharmgkbrs587782799
gwascentralrs587782799
openSNPrs587782799
23andMers587782799
23andMe allrs587782799
SNP Nexus

SNPshotrs587782799
SNPdbers587782799
MSV3drs587782799
GWAS Ctlgrs587782799
Max Magnitude0
ClinVar
Risk rs587782799(;)
Alt rs587782799(;)
Reference rs587782799(AGTT;AGTT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32914718_32914721delGTTA
CLNSRC
CLNACC RCV000132354.2,