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rs397509316

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509316(-;-)
Make rs397509316(-;A)
Make rs397509316(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094762
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509316
ebirs397509316
HLIrs397509316
Exacrs397509316
Varsomers397509316
Maprs397509316
PheGenIrs397509316
hapmaprs397509316
1000 genomesrs397509316
hgdprs397509316
ensemblrs397509316
gopubmedrs397509316
geneviewrs397509316
scholarrs397509316
googlers397509316
pharmgkbrs397509316
gwascentralrs397509316
openSNPrs397509316
23andMers397509316
23andMe allrs397509316
SNP Nexus

SNPshotrs397509316
SNPdbers397509316
MSV3drs397509316
GWAS Ctlgrs397509316
Max Magnitude0
ClinVar
Risk rs397509316(AC,AGC;AC,AGC)
Alt rs397509316(AC,AGC;AC,AGC)
Reference rs397509316(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246779_41246780insCT; NC_000017.10:g.41246779_41246780insT
CLNSRC ClinVar
CLNACC RCV000049126.2, RCV000049125.2,