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rs397509306

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509306(A;G)
Make rs397509306(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43095848
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509306
ebirs397509306
HLIrs397509306
Exacrs397509306
Varsomers397509306
Maprs397509306
PheGenIrs397509306
hapmaprs397509306
1000 genomesrs397509306
hgdprs397509306
ensemblrs397509306
gopubmedrs397509306
geneviewrs397509306
scholarrs397509306
googlers397509306
pharmgkbrs397509306
gwascentralrs397509306
openSNPrs397509306
23andMers397509306
23andMe allrs397509306
SNP Nexus

SNPshotrs397509306
SNPdbers397509306
MSV3drs397509306
GWAS Ctlgrs397509306
Max Magnitude0
ClinVar
Risk rs397509306(G;G)
Alt rs397509306(G;G)
Reference rs397509306(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.41247865T>C
CLNSRC ClinVar
CLNACC RCV000049084.2,