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rs397509093

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GTAA;GTAA) 0 common in clinvar
Make rs397509093(-;-)
Make rs397509093(-;GTAA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091833
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509093
ebirs397509093
HLIrs397509093
Exacrs397509093
Varsomers397509093
Maprs397509093
PheGenIrs397509093
hapmaprs397509093
1000 genomesrs397509093
hgdprs397509093
ensemblrs397509093
gopubmedrs397509093
geneviewrs397509093
scholarrs397509093
googlers397509093
pharmgkbrs397509093
gwascentralrs397509093
openSNPrs397509093
23andMers397509093
23andMe allrs397509093
SNP Nexus

SNPshotrs397509093
SNPdbers397509093
MSV3drs397509093
GWAS Ctlgrs397509093
Max Magnitude0
ClinVar
Risk rs397509093(;)
Alt rs397509093(;)
Reference rs397509093(GTAA;GTAA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243850_41243853delTTAC
CLNSRC ClinVar
CLNACC RCV000048284.2,