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rs397509205

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509205(G;T)
Make rs397509205(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43070984
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509205
ebirs397509205
HLIrs397509205
Exacrs397509205
Varsomers397509205
Maprs397509205
PheGenIrs397509205
hapmaprs397509205
1000 genomesrs397509205
hgdprs397509205
ensemblrs397509205
gopubmedrs397509205
geneviewrs397509205
scholarrs397509205
googlers397509205
pharmgkbrs397509205
gwascentralrs397509205
openSNPrs397509205
23andMers397509205
23andMe allrs397509205
SNP Nexus

SNPshotrs397509205
SNPdbers397509205
MSV3drs397509205
GWAS Ctlgrs397509205
Max Magnitude0
ClinVar
Risk rs397509205(T;T)
Alt rs397509205(T;T)
Reference rs397509205(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41223001C>A
CLNSRC ClinVar
CLNACC RCV000048694.2,