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rs397509206

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs397509206(-;-)
Make rs397509206(-;CT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43099828
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509206
ebirs397509206
HLIrs397509206
Exacrs397509206
Varsomers397509206
Maprs397509206
PheGenIrs397509206
hapmaprs397509206
1000 genomesrs397509206
hgdprs397509206
ensemblrs397509206
gopubmedrs397509206
geneviewrs397509206
scholarrs397509206
googlers397509206
pharmgkbrs397509206
gwascentralrs397509206
openSNPrs397509206
23andMers397509206
23andMe allrs397509206
SNP Nexus

SNPshotrs397509206
SNPdbers397509206
MSV3drs397509206
GWAS Ctlgrs397509206
Max Magnitude0
ClinVar
Risk rs397509206(;)
Alt rs397509206(;)
Reference rs397509206(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.41251845_41251846delAG
CLNSRC ClinVar
CLNACC RCV000048700.2,