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rs397508935

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CAAG;CAAG) 0 common in clinvar
Make rs397508935(-;-)
Make rs397508935(-;CAAG)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093465
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508935
ebirs397508935
HLIrs397508935
Exacrs397508935
Varsomers397508935
Maprs397508935
PheGenIrs397508935
hapmaprs397508935
1000 genomesrs397508935
hgdprs397508935
ensemblrs397508935
gopubmedrs397508935
geneviewrs397508935
scholarrs397508935
googlers397508935
pharmgkbrs397508935
gwascentralrs397508935
openSNPrs397508935
23andMers397508935
23andMe allrs397508935
SNP Nexus

SNPshotrs397508935
SNPdbers397508935
MSV3drs397508935
GWAS Ctlgrs397508935
Max Magnitude0
ClinVar
Risk rs397508935(;)
Alt rs397508935(;)
Reference rs397508935(CAAG;CAAG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245482_41245485delCTTG
CLNSRC ClinVar
CLNACC RCV000047697.2,