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rs397509336

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509336(-;-)
Make rs397509336(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094607
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509336
ebirs397509336
HLIrs397509336
Exacrs397509336
Varsomers397509336
Maprs397509336
PheGenIrs397509336
hapmaprs397509336
1000 genomesrs397509336
hgdprs397509336
ensemblrs397509336
gopubmedrs397509336
geneviewrs397509336
scholarrs397509336
googlers397509336
pharmgkbrs397509336
gwascentralrs397509336
openSNPrs397509336
23andMers397509336
23andMe allrs397509336
SNP Nexus

SNPshotrs397509336
SNPdbers397509336
MSV3drs397509336
GWAS Ctlgrs397509336
Max Magnitude0
ClinVar
Risk rs397509336(;)
Alt rs397509336(;)
Reference rs397509336(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.41246624delG
CLNSRC ClinVar
CLNACC RCV000049190.2,