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rs769152395

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs769152395(A;G)
Make rs769152395(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32319075
GeneBRCA2
is asnp
is mentioned by
dbSNPrs769152395
ebirs769152395
HLIrs769152395
Exacrs769152395
Varsomers769152395
Maprs769152395
PheGenIrs769152395
hapmaprs769152395
1000 genomesrs769152395
hgdprs769152395
ensemblrs769152395
gopubmedrs769152395
geneviewrs769152395
scholarrs769152395
googlers769152395
pharmgkbrs769152395
gwascentralrs769152395
openSNPrs769152395
23andMers769152395
23andMe allrs769152395
SNP Nexus

SNPshotrs769152395
SNPdbers769152395
MSV3drs769152395
GWAS Ctlgrs769152395
Max Magnitude0
ClinVar
Risk rs769152395(G;G)
Alt rs769152395(G;G)
Reference rs769152395(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32893212A>G
CLNSRC
CLNACC RCV000167275.1,