Have questions? Visit https://www.reddit.com/r/SNPedia

rs876657678

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657678(C;T)
Make rs876657678(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32337542
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876657678
ebirs876657678
HLIrs876657678
Exacrs876657678
Varsomers876657678
Maprs876657678
PheGenIrs876657678
hapmaprs876657678
1000 genomesrs876657678
hgdprs876657678
ensemblrs876657678
gopubmedrs876657678
geneviewrs876657678
scholarrs876657678
googlers876657678
pharmgkbrs876657678
gwascentralrs876657678
openSNPrs876657678
23andMers876657678
23andMe allrs876657678
SNP Nexus

SNPshotrs876657678
SNPdbers876657678
MSV3drs876657678
GWAS Ctlgrs876657678
Max Magnitude0
ClinVar
Risk rs876657678(T;T)
Alt rs876657678(T;T)
Reference rs876657678(C;C)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32911679C>T
CLNSRC
CLNACC RCV000218286.1,