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rs876660524

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;G) 6 BRCA2 variant considered pathogenic for breast cancer
(G;G) 0 common in clinvar


Make rs876660524(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339431
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660524
dbSNP (classic)rs876660524
ClinGenrs876660524
ebirs876660524
HLIrs876660524
Exacrs876660524
Gnomadrs876660524
Varsomers876660524
LitVarrs876660524
Maprs876660524
PheGenIrs876660524
Biobankrs876660524
1000 genomesrs876660524
hgdprs876660524
ensemblrs876660524
geneviewrs876660524
scholarrs876660524
googlers876660524
pharmgkbrs876660524
gwascentralrs876660524
openSNPrs876660524
23andMers876660524
SNPshotrs876660524
SNPdbers876660524
MSV3drs876660524
GWAS Ctlgrs876660524
Max Magnitude6

aka c.5076delG

ClinVar
Risk rs876660524(-;-)
Alt rs876660524(-;-)
Reference Rs876660524(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32913568delG
CLNSRC
CLNACC RCV000220340.1,