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rs397509005

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509005(-;-)
Make rs397509005(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092803
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509005
ebirs397509005
HLIrs397509005
Exacrs397509005
Varsomers397509005
Maprs397509005
PheGenIrs397509005
hapmaprs397509005
1000 genomesrs397509005
hgdprs397509005
ensemblrs397509005
gopubmedrs397509005
geneviewrs397509005
scholarrs397509005
googlers397509005
pharmgkbrs397509005
gwascentralrs397509005
openSNPrs397509005
23andMers397509005
23andMe allrs397509005
SNP Nexus

SNPshotrs397509005
SNPdbers397509005
MSV3drs397509005
GWAS Ctlgrs397509005
Max Magnitude0
ClinVar
Risk rs397509005(;)
Alt rs397509005(;)
Reference rs397509005(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.41244820delG
CLNSRC ClinVar
CLNACC RCV000047950.2,