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rs397509036

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GCAATATTAA;GCAATATTAA) 0 common in clinvar
Make rs397509036(-;-)
Make rs397509036(-;GCAATATTAA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092397
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509036
ebirs397509036
HLIrs397509036
Exacrs397509036
Varsomers397509036
Maprs397509036
PheGenIrs397509036
hapmaprs397509036
1000 genomesrs397509036
hgdprs397509036
ensemblrs397509036
gopubmedrs397509036
geneviewrs397509036
scholarrs397509036
googlers397509036
pharmgkbrs397509036
gwascentralrs397509036
openSNPrs397509036
23andMers397509036
23andMe allrs397509036
SNP Nexus

SNPshotrs397509036
SNPdbers397509036
MSV3drs397509036
GWAS Ctlgrs397509036
Max Magnitude0
ClinVar
Risk rs397509036(;)
Alt rs397509036(;)
Reference rs397509036(GCAATATTAA;GCAATATTAA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244414_41244423delTTAATATTGC
CLNSRC ClinVar
CLNACC RCV000048076.2,