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rs397509070

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509070(-;-)
Make rs397509070(-;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092063
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509070
ebirs397509070
HLIrs397509070
Exacrs397509070
Varsomers397509070
Maprs397509070
PheGenIrs397509070
hapmaprs397509070
1000 genomesrs397509070
hgdprs397509070
ensemblrs397509070
gopubmedrs397509070
geneviewrs397509070
scholarrs397509070
googlers397509070
pharmgkbrs397509070
gwascentralrs397509070
openSNPrs397509070
23andMers397509070
23andMe allrs397509070
SNP Nexus

SNPshotrs397509070
SNPdbers397509070
MSV3drs397509070
GWAS Ctlgrs397509070
Max Magnitude0
ClinVar
Risk rs397509070(;)
Alt rs397509070(;)
Reference rs397509070(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.41244080delA
CLNSRC ClinVar
CLNACC RCV000048205.2,