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rs397508884

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508884(-;-)
Make rs397508884(-;C)
Make rs397508884(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093965
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508884
ebirs397508884
HLIrs397508884
Exacrs397508884
Varsomers397508884
Maprs397508884
PheGenIrs397508884
hapmaprs397508884
1000 genomesrs397508884
hgdprs397508884
ensemblrs397508884
gopubmedrs397508884
geneviewrs397508884
scholarrs397508884
googlers397508884
pharmgkbrs397508884
gwascentralrs397508884
openSNPrs397508884
23andMers397508884
23andMe allrs397508884
SNP Nexus

SNPshotrs397508884
SNPdbers397508884
MSV3drs397508884
GWAS Ctlgrs397508884
Max Magnitude0
ClinVar
Risk rs397508884(C;C)
Alt rs397508884(C;C)
Reference rs397508884(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245982_41245983insG
CLNSRC ClinVar
CLNACC RCV000047526.2,