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rs397509308

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509308(A;A)
Make rs397509308(A;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094853
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509308
ebirs397509308
HLIrs397509308
Exacrs397509308
Varsomers397509308
Maprs397509308
PheGenIrs397509308
hapmaprs397509308
1000 genomesrs397509308
hgdprs397509308
ensemblrs397509308
gopubmedrs397509308
geneviewrs397509308
scholarrs397509308
googlers397509308
pharmgkbrs397509308
gwascentralrs397509308
openSNPrs397509308
23andMers397509308
23andMe allrs397509308
SNP Nexus

SNPshotrs397509308
SNPdbers397509308
MSV3drs397509308
GWAS Ctlgrs397509308
Max Magnitude0
ClinVar
Risk rs397509308(A;A)
Alt rs397509308(A;A)
Reference rs397509308(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246870A>T
CLNSRC ClinVar
CLNACC RCV000049093.2,