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rs397509164

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509164(-;-)
Make rs397509164(-;AGAA)
Make rs397509164(AGAA;AGAA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43082422
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509164
ebirs397509164
HLIrs397509164
Exacrs397509164
Varsomers397509164
Maprs397509164
PheGenIrs397509164
hapmaprs397509164
1000 genomesrs397509164
hgdprs397509164
ensemblrs397509164
gopubmedrs397509164
geneviewrs397509164
scholarrs397509164
googlers397509164
pharmgkbrs397509164
gwascentralrs397509164
openSNPrs397509164
23andMers397509164
23andMe allrs397509164
SNP Nexus

SNPshotrs397509164
SNPdbers397509164
MSV3drs397509164
GWAS Ctlgrs397509164
Max Magnitude0
ClinVar
Risk rs397509164(AGAA;AGAA)
Alt rs397509164(AGAA;AGAA)
Reference rs397509164(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41234440_41234443dupTTCT
CLNSRC
CLNACC RCV000048527.2,