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rs397509077

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509077(-;-)
Make rs397509077(-;A)
Make rs397509077(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092027
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509077
ebirs397509077
HLIrs397509077
Exacrs397509077
Varsomers397509077
Maprs397509077
PheGenIrs397509077
hapmaprs397509077
1000 genomesrs397509077
hgdprs397509077
ensemblrs397509077
gopubmedrs397509077
geneviewrs397509077
scholarrs397509077
googlers397509077
pharmgkbrs397509077
gwascentralrs397509077
openSNPrs397509077
23andMers397509077
23andMe allrs397509077
SNP Nexus

SNPshotrs397509077
SNPdbers397509077
MSV3drs397509077
GWAS Ctlgrs397509077
Max Magnitude0
ClinVar
Risk rs397509077(A;A)
Alt rs397509077(A;A)
Reference rs397509077(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244045dupT
CLNSRC ClinVar
CLNACC RCV000048218.2,