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rs397508839

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs397508839(-;-)
Make rs397508839(-;AC)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094408
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508839
ebirs397508839
HLIrs397508839
Exacrs397508839
Varsomers397508839
Maprs397508839
PheGenIrs397508839
hapmaprs397508839
1000 genomesrs397508839
hgdprs397508839
ensemblrs397508839
gopubmedrs397508839
geneviewrs397508839
scholarrs397508839
googlers397508839
pharmgkbrs397508839
gwascentralrs397508839
openSNPrs397508839
23andMers397508839
23andMe allrs397508839
SNP Nexus

SNPshotrs397508839
SNPdbers397508839
MSV3drs397508839
GWAS Ctlgrs397508839
Max Magnitude0
ClinVar
Risk rs397508839(;)
Alt rs397508839(;)
Reference rs397508839(AC;AC)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246425_41246426delGT
CLNSRC ClinVar
CLNACC RCV000047352.2,