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rs876661056

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661056(G;T)
Make rs876661056(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339489
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876661056
ebirs876661056
HLIrs876661056
Exacrs876661056
Varsomers876661056
Maprs876661056
PheGenIrs876661056
hapmaprs876661056
1000 genomesrs876661056
hgdprs876661056
ensemblrs876661056
gopubmedrs876661056
geneviewrs876661056
scholarrs876661056
googlers876661056
pharmgkbrs876661056
gwascentralrs876661056
openSNPrs876661056
23andMers876661056
23andMe allrs876661056
SNP Nexus

SNPshotrs876661056
SNPdbers876661056
MSV3drs876661056
GWAS Ctlgrs876661056
Max Magnitude0
ClinVar
Risk rs876661056(T;T)
Alt rs876661056(T;T)
Reference rs876661056(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32913626G>T
CLNSRC
CLNACC RCV000220651.1,