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

rs760815829

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs760815829(C;T)
Make rs760815829(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32332667
GeneBRCA2
is asnp
is mentioned by
dbSNPrs760815829
ebirs760815829
HLIrs760815829
Exacrs760815829
Varsomers760815829
Maprs760815829
PheGenIrs760815829
hapmaprs760815829
1000 genomesrs760815829
hgdprs760815829
ensemblrs760815829
gopubmedrs760815829
geneviewrs760815829
scholarrs760815829
googlers760815829
pharmgkbrs760815829
gwascentralrs760815829
openSNPrs760815829
23andMers760815829
23andMe allrs760815829
SNP Nexus

SNPshotrs760815829
SNPdbers760815829
MSV3drs760815829
GWAS Ctlgrs760815829
Max Magnitude0
ClinVar
Risk rs760815829(T;T)
Alt rs760815829(T;T)
Reference rs760815829(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.32906804C>T
CLNSRC
CLNACC RCV000227783.1,