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rs397509161

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs397509161(-;-)
Make rs397509161(-;CT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43082453
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509161
ebirs397509161
HLIrs397509161
Exacrs397509161
Varsomers397509161
Maprs397509161
PheGenIrs397509161
hapmaprs397509161
1000 genomesrs397509161
hgdprs397509161
ensemblrs397509161
gopubmedrs397509161
geneviewrs397509161
scholarrs397509161
googlers397509161
pharmgkbrs397509161
gwascentralrs397509161
openSNPrs397509161
23andMers397509161
23andMe allrs397509161
SNP Nexus

SNPshotrs397509161
SNPdbers397509161
MSV3drs397509161
GWAS Ctlgrs397509161
Max Magnitude0
ClinVar
Risk rs397509161(;)
Alt rs397509161(;)
Reference rs397509161(CT;CT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41234470_41234471delAG
CLNSRC ClinVar
CLNACC RCV000048518.2,