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rs397508862

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508862(-;-)
Make rs397508862(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094157
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508862
ebirs397508862
HLIrs397508862
Exacrs397508862
Varsomers397508862
Maprs397508862
PheGenIrs397508862
hapmaprs397508862
1000 genomesrs397508862
hgdprs397508862
ensemblrs397508862
gopubmedrs397508862
geneviewrs397508862
scholarrs397508862
googlers397508862
pharmgkbrs397508862
gwascentralrs397508862
openSNPrs397508862
23andMers397508862
23andMe allrs397508862
SNP Nexus

SNPshotrs397508862
SNPdbers397508862
MSV3drs397508862
GWAS Ctlgrs397508862
Max Magnitude0

c.1374delC (p.Asp458Glufs)

ClinVar clinical significance not provided


ClinVar
Risk rs397508862(;)
Alt rs397508862(;)
Reference rs397508862(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246174delG
CLNSRC ClinVar
CLNACC RCV000047445.2,