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rs397508834

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508834(-;-)
Make rs397508834(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094440
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508834
ebirs397508834
HLIrs397508834
Exacrs397508834
Varsomers397508834
Maprs397508834
PheGenIrs397508834
hapmaprs397508834
1000 genomesrs397508834
hgdprs397508834
ensemblrs397508834
gopubmedrs397508834
geneviewrs397508834
scholarrs397508834
googlers397508834
pharmgkbrs397508834
gwascentralrs397508834
openSNPrs397508834
23andMers397508834
23andMe allrs397508834
SNP Nexus

SNPshotrs397508834
SNPdbers397508834
MSV3drs397508834
GWAS Ctlgrs397508834
Max Magnitude0
ClinVar
Risk rs397508834(;)
Alt rs397508834(;)
Reference rs397508834(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.41246457delG
CLNSRC ClinVar
CLNACC RCV000047337.2,