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rs397508899

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508899(-;-)
Make rs397508899(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093831
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508899
ebirs397508899
HLIrs397508899
Exacrs397508899
Varsomers397508899
Maprs397508899
PheGenIrs397508899
hapmaprs397508899
1000 genomesrs397508899
hgdprs397508899
ensemblrs397508899
gopubmedrs397508899
geneviewrs397508899
scholarrs397508899
googlers397508899
pharmgkbrs397508899
gwascentralrs397508899
openSNPrs397508899
23andMers397508899
23andMe allrs397508899
SNP Nexus

SNPshotrs397508899
SNPdbers397508899
MSV3drs397508899
GWAS Ctlgrs397508899
Max Magnitude0
ClinVar
Risk rs397508899(;)
Alt rs397508899(;)
Reference rs397508899(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245848delT
CLNSRC ClinVar
CLNACC RCV000047562.2,