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rs397509262

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs397509262(-;-)
Make rs397509262(-;AT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43051071
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509262
ebirs397509262
HLIrs397509262
Exacrs397509262
Varsomers397509262
Maprs397509262
PheGenIrs397509262
hapmaprs397509262
1000 genomesrs397509262
hgdprs397509262
ensemblrs397509262
gopubmedrs397509262
geneviewrs397509262
scholarrs397509262
googlers397509262
pharmgkbrs397509262
gwascentralrs397509262
openSNPrs397509262
23andMers397509262
23andMe allrs397509262
SNP Nexus

SNPshotrs397509262
SNPdbers397509262
MSV3drs397509262
GWAS Ctlgrs397509262
Max Magnitude0
ClinVar
Risk rs397509262(;)
Alt rs397509262(;)
Reference rs397509262(AT;AT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41203088_41203089delAT
CLNSRC ClinVar
CLNACC RCV000048929.2,