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rs397509004

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509004(C;T)
Make rs397509004(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092803
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509004
ebirs397509004
HLIrs397509004
Exacrs397509004
Varsomers397509004
Maprs397509004
PheGenIrs397509004
hapmaprs397509004
1000 genomesrs397509004
hgdprs397509004
ensemblrs397509004
gopubmedrs397509004
geneviewrs397509004
scholarrs397509004
googlers397509004
pharmgkbrs397509004
gwascentralrs397509004
openSNPrs397509004
23andMers397509004
23andMe allrs397509004
SNP Nexus

SNPshotrs397509004
SNPdbers397509004
MSV3drs397509004
GWAS Ctlgrs397509004
Max Magnitude0
ClinVar
Risk rs397509004(T;T)
Alt rs397509004(T;T)
Reference rs397509004(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.41244820G>A
CLNSRC ClinVar
CLNACC RCV000047949.2,