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rs876661062

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661062(C;T)
Make rs876661062(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339006
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876661062
ClinGenrs876661062
ebirs876661062
HLIrs876661062
Exacrs876661062
Varsomers876661062
Maprs876661062
PheGenIrs876661062
hapmaprs876661062
1000 genomesrs876661062
hgdprs876661062
ensemblrs876661062
gopubmedrs876661062
geneviewrs876661062
scholarrs876661062
googlers876661062
pharmgkbrs876661062
gwascentralrs876661062
openSNPrs876661062
23andMers876661062
23andMe allrs876661062
SNP Nexus

SNPshotrs876661062
SNPdbers876661062
MSV3drs876661062
GWAS Ctlgrs876661062
Max Magnitude0
ClinVar
Risk rs876661062(T;T)
Alt rs876661062(T;T)
Reference Rs876661062(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32913143C>T
CLNSRC
CLNACC RCV000219028.1,