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rs876658643

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658643(-;-)
Make rs876658643(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32394710
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658643
dbSNP (classic)rs876658643
ClinGenrs876658643
ebirs876658643
HLIrs876658643
Exacrs876658643
Gnomadrs876658643
Varsomers876658643
LitVarrs876658643
Maprs876658643
PheGenIrs876658643
Biobankrs876658643
1000 genomesrs876658643
hgdprs876658643
ensemblrs876658643
geneviewrs876658643
scholarrs876658643
googlers876658643
pharmgkbrs876658643
gwascentralrs876658643
openSNPrs876658643
23andMers876658643
SNPshotrs876658643
SNPdbers876658643
MSV3drs876658643
GWAS Ctlgrs876658643
Max Magnitude0
ClinVar
Risk rs876658643(-;-)
Alt rs876658643(-;-)
Reference Rs876658643(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32968847delT
CLNSRC
CLNACC RCV000222200.1,