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

rs273899696

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs273899696(A;A)
Make rs273899696(A;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092505
GeneBRCA1
is asnp
is mentioned by
dbSNPrs273899696
ebirs273899696
HLIrs273899696
Exacrs273899696
Varsomers273899696
Maprs273899696
PheGenIrs273899696
hapmaprs273899696
1000 genomesrs273899696
hgdprs273899696
ensemblrs273899696
gopubmedrs273899696
geneviewrs273899696
scholarrs273899696
googlers273899696
pharmgkbrs273899696
gwascentralrs273899696
openSNPrs273899696
23andMers273899696
23andMe allrs273899696
SNP Nexus

SNPshotrs273899696
SNPdbers273899696
MSV3drs273899696
GWAS Ctlgrs273899696
Max Magnitude0
ClinVar
Risk rs273899696(A;A)
Alt rs273899696(A;A)
Reference rs273899696(C;C)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41244522G>T
CLNSRC ClinVar
CLNACC RCV000048052.2, RCV000111985.1,