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

rs368796923

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs368796923(A;A)
Make rs368796923(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position61799200
GeneBRIP1
is asnp
is mentioned by
dbSNPrs368796923
ebirs368796923
HLIrs368796923
Exacrs368796923
Varsomers368796923
Maprs368796923
PheGenIrs368796923
hapmaprs368796923
1000 genomesrs368796923
hgdprs368796923
ensemblrs368796923
gopubmedrs368796923
geneviewrs368796923
scholarrs368796923
googlers368796923
pharmgkbrs368796923
gwascentralrs368796923
openSNPrs368796923
23andMers368796923
23andMe allrs368796923
SNP Nexus

SNPshotrs368796923
SNPdbers368796923
MSV3drs368796923
GWAS Ctlgrs368796923
Max Magnitude0
ClinVar
Risk rs368796923(A;A)
Alt rs368796923(A;A)
Reference rs368796923(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.59876561G>A
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000129878.2,