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rs876659318

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659318(-;-)
Make rs876659318(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32336611
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659318
dbSNP (old)rs876659318
ClinGenrs876659318
ebirs876659318
HLIrs876659318
Exacrs876659318
Gnomadrs876659318
Varsomers876659318
Maprs876659318
PheGenIrs876659318
Biobankrs876659318
1000 genomesrs876659318
hgdprs876659318
ensemblrs876659318
gopubmedrs876659318
geneviewrs876659318
scholarrs876659318
googlers876659318
pharmgkbrs876659318
gwascentralrs876659318
openSNPrs876659318
23andMers876659318
23andMe allrs876659318
SNP Nexus

SNPshotrs876659318
SNPdbers876659318
MSV3drs876659318
GWAS Ctlgrs876659318
Max Magnitude0
ClinVar
Risk rs876659318(-;-)
Alt rs876659318(-;-)
Reference Rs876659318(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32910748delC
CLNSRC
CLNACC RCV000220476.1,