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

rs398122661

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122661(G;T)
Make rs398122661(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43104919
GeneBRCA1
is asnp
is mentioned by
dbSNPrs398122661
ebirs398122661
HLIrs398122661
Exacrs398122661
Varsomers398122661
Maprs398122661
PheGenIrs398122661
hapmaprs398122661
1000 genomesrs398122661
hgdprs398122661
ensemblrs398122661
gopubmedrs398122661
geneviewrs398122661
scholarrs398122661
googlers398122661
pharmgkbrs398122661
gwascentralrs398122661
openSNPrs398122661
23andMers398122661
23andMe allrs398122661
SNP Nexus

SNPshotrs398122661
SNPdbers398122661
MSV3drs398122661
GWAS Ctlgrs398122661
Max Magnitude0
ClinVar
Risk rs398122661(T;T)
Alt rs398122661(T;T)
Reference rs398122661(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41256936C>A
CLNSRC ClinVar
CLNACC RCV000077108.3,