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rs397508894

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508894(G;T)
Make rs397508894(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093871
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508894
ebirs397508894
HLIrs397508894
Exacrs397508894
Varsomers397508894
Maprs397508894
PheGenIrs397508894
hapmaprs397508894
1000 genomesrs397508894
hgdprs397508894
ensemblrs397508894
gopubmedrs397508894
geneviewrs397508894
scholarrs397508894
googlers397508894
pharmgkbrs397508894
gwascentralrs397508894
openSNPrs397508894
23andMers397508894
23andMe allrs397508894
SNP Nexus

SNPshotrs397508894
SNPdbers397508894
MSV3drs397508894
GWAS Ctlgrs397508894
Max Magnitude0
ClinVar
Risk rs397508894(T;T)
Alt rs397508894(T;T)
Reference rs397508894(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.41245888C>A
CLNSRC ClinVar
CLNACC RCV000047553.2,