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rs397509214

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509214(A;A)
Make rs397509214(A;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43067700
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509214
ebirs397509214
HLIrs397509214
Exacrs397509214
Varsomers397509214
Maprs397509214
PheGenIrs397509214
hapmaprs397509214
1000 genomesrs397509214
hgdprs397509214
ensemblrs397509214
gopubmedrs397509214
geneviewrs397509214
scholarrs397509214
googlers397509214
pharmgkbrs397509214
gwascentralrs397509214
openSNPrs397509214
23andMers397509214
23andMe allrs397509214
SNP Nexus

SNPshotrs397509214
SNPdbers397509214
MSV3drs397509214
GWAS Ctlgrs397509214
Max Magnitude0
ClinVar
Risk rs397509214(A;A)
Alt rs397509214(A;A)
Reference rs397509214(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.41219717A>T
CLNSRC ClinVar
CLNACC RCV000048728.2,