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

rs397508877

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508877(A;T)
Make rs397508877(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094018
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508877
ebirs397508877
HLIrs397508877
Exacrs397508877
Varsomers397508877
Maprs397508877
PheGenIrs397508877
hapmaprs397508877
1000 genomesrs397508877
hgdprs397508877
ensemblrs397508877
gopubmedrs397508877
geneviewrs397508877
scholarrs397508877
googlers397508877
pharmgkbrs397508877
gwascentralrs397508877
openSNPrs397508877
23andMers397508877
23andMe allrs397508877
SNP Nexus

SNPshotrs397508877
SNPdbers397508877
MSV3drs397508877
GWAS Ctlgrs397508877
Max Magnitude0
ClinVar
Risk rs397508877(T;T)
Alt rs397508877(T;T)
Reference rs397508877(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246035T>A
CLNSRC ClinVar
CLNACC RCV000047509.2,