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rs397509234

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAAATGCTGAATGA;AAAATGCTGAATGA) 0 common in clinvar
Make rs397509234(-;-)
Make rs397509234(-;AAAATGCTGAATGA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43063334
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509234
ebirs397509234
HLIrs397509234
Exacrs397509234
Varsomers397509234
Maprs397509234
PheGenIrs397509234
hapmaprs397509234
1000 genomesrs397509234
hgdprs397509234
ensemblrs397509234
gopubmedrs397509234
geneviewrs397509234
scholarrs397509234
googlers397509234
pharmgkbrs397509234
gwascentralrs397509234
openSNPrs397509234
23andMers397509234
23andMe allrs397509234
SNP Nexus

SNPshotrs397509234
SNPdbers397509234
MSV3drs397509234
GWAS Ctlgrs397509234
Max Magnitude0
ClinVar
Risk rs397509234(;)
Alt rs397509234(;)
Reference rs397509234(AAAATGCTGAATGA;AAAATGCTGAATGA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41215351_41215364delTCATTCAGCATTTT
CLNSRC ClinVar
CLNACC RCV000048845.2,