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rs397508977

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508977(-;-)
Make rs397508977(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092980
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508977
ebirs397508977
HLIrs397508977
Exacrs397508977
Varsomers397508977
Maprs397508977
PheGenIrs397508977
hapmaprs397508977
1000 genomesrs397508977
hgdprs397508977
ensemblrs397508977
gopubmedrs397508977
geneviewrs397508977
scholarrs397508977
googlers397508977
pharmgkbrs397508977
gwascentralrs397508977
openSNPrs397508977
23andMers397508977
23andMe allrs397508977
SNP Nexus

SNPshotrs397508977
SNPdbers397508977
MSV3drs397508977
GWAS Ctlgrs397508977
Max Magnitude0
ClinVar
Risk rs397508977(;)
Alt rs397508977(;)
Reference rs397508977(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244997delC
CLNSRC ClinVar
CLNACC RCV000047873.2,