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rs397509285

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509285(A;G)
Make rs397509285(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43047662
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509285
ebirs397509285
HLIrs397509285
Exacrs397509285
Varsomers397509285
Maprs397509285
PheGenIrs397509285
hapmaprs397509285
1000 genomesrs397509285
hgdprs397509285
ensemblrs397509285
gopubmedrs397509285
geneviewrs397509285
scholarrs397509285
googlers397509285
pharmgkbrs397509285
gwascentralrs397509285
openSNPrs397509285
23andMers397509285
23andMe allrs397509285
SNP Nexus

SNPshotrs397509285
SNPdbers397509285
MSV3drs397509285
GWAS Ctlgrs397509285
Max Magnitude0
ClinVar
Risk rs397509285(G;G)
Alt rs397509285(G;G)
Reference rs397509285(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41199679T>C
CLNSRC ClinVar
CLNACC RCV000048998.2,