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rs587781803

From SNPedia

Orientationplus
Geno Mag Summary
(AGAAG;AGAAG) 0 common in clinvar
Make rs587781803(-;-)
Make rs587781803(-;AAGAG)
Make rs587781803(AAGAG;AAGAG)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32341171
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587781803
ebirs587781803
HLIrs587781803
Exacrs587781803
Varsomers587781803
Maprs587781803
PheGenIrs587781803
hapmaprs587781803
1000 genomesrs587781803
hgdprs587781803
ensemblrs587781803
gopubmedrs587781803
geneviewrs587781803
scholarrs587781803
googlers587781803
pharmgkbrs587781803
gwascentralrs587781803
openSNPrs587781803
23andMers587781803
23andMe allrs587781803
SNP Nexus

SNPshotrs587781803
SNPdbers587781803
MSV3drs587781803
GWAS Ctlgrs587781803
Max Magnitude0
ClinVar
Risk rs587781803(;)
Alt rs587781803(;)
Reference rs587781803(AGAAG;AGAAG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 1 Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32915308_32915312delAAGAG
CLNSRC
CLNACC RCV000130069.2, RCV000210139.1, RCV000210971.1,