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rs397508876

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAAGC;AAAGC) 0 common in clinvar
Make rs397508876(-;-)
Make rs397508876(-;AAAGC)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094021
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508876
ebirs397508876
HLIrs397508876
Exacrs397508876
Varsomers397508876
Maprs397508876
PheGenIrs397508876
hapmaprs397508876
1000 genomesrs397508876
hgdprs397508876
ensemblrs397508876
gopubmedrs397508876
geneviewrs397508876
scholarrs397508876
googlers397508876
pharmgkbrs397508876
gwascentralrs397508876
openSNPrs397508876
23andMers397508876
23andMe allrs397508876
SNP Nexus

SNPshotrs397508876
SNPdbers397508876
MSV3drs397508876
GWAS Ctlgrs397508876
Max Magnitude0
ClinVar
Risk rs397508876(;)
Alt rs397508876(;)
Reference rs397508876(AAAGC;AAAGC)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246038_41246042delGCTTT
CLNSRC ClinVar
CLNACC RCV000047501.2,