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rs876661045

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661045(C;C)
Make rs876661045(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32325186
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876661045
ebirs876661045
HLIrs876661045
Exacrs876661045
Varsomers876661045
Maprs876661045
PheGenIrs876661045
hapmaprs876661045
1000 genomesrs876661045
hgdprs876661045
ensemblrs876661045
gopubmedrs876661045
geneviewrs876661045
scholarrs876661045
googlers876661045
pharmgkbrs876661045
gwascentralrs876661045
openSNPrs876661045
23andMers876661045
23andMe allrs876661045
SNP Nexus

SNPshotrs876661045
SNPdbers876661045
MSV3drs876661045
GWAS Ctlgrs876661045
Max Magnitude0
ClinVar
Risk rs876661045(C;C)
Alt rs876661045(C;C)
Reference rs876661045(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32899323T>C
CLNSRC
CLNACC RCV000221962.1,