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rs397509265

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509265(G;G)
Make rs397509265(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43049197
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509265
ebirs397509265
HLIrs397509265
Exacrs397509265
Varsomers397509265
Maprs397509265
PheGenIrs397509265
hapmaprs397509265
1000 genomesrs397509265
hgdprs397509265
ensemblrs397509265
gopubmedrs397509265
geneviewrs397509265
scholarrs397509265
googlers397509265
pharmgkbrs397509265
gwascentralrs397509265
openSNPrs397509265
23andMers397509265
23andMe allrs397509265
SNP Nexus

SNPshotrs397509265
SNPdbers397509265
MSV3drs397509265
GWAS Ctlgrs397509265
Max Magnitude0
ClinVar
Risk rs397509265(G;G)
Alt rs397509265(G;G)
Reference rs397509265(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.41201214A>C
CLNSRC ClinVar
CLNACC RCV000048943.2,