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rs397509321

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509321(A;T)
Make rs397509321(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094741
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509321
ebirs397509321
HLIrs397509321
Exacrs397509321
Varsomers397509321
Maprs397509321
PheGenIrs397509321
hapmaprs397509321
1000 genomesrs397509321
hgdprs397509321
ensemblrs397509321
gopubmedrs397509321
geneviewrs397509321
scholarrs397509321
googlers397509321
pharmgkbrs397509321
gwascentralrs397509321
openSNPrs397509321
23andMers397509321
23andMe allrs397509321
SNP Nexus

SNPshotrs397509321
SNPdbers397509321
MSV3drs397509321
GWAS Ctlgrs397509321
Max Magnitude0
ClinVar
Risk rs397509321(G,T;G,T)
Alt rs397509321(G,T;G,T)
Reference rs397509321(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.41246758T>A
CLNSRC ClinVar
CLNACC RCV000049135.2,