Have questions? Visit https://www.reddit.com/r/SNPedia

rs397509134

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;TAATCAA) 6 BRCA1 variant considered pathogenic for breast cancer
(TAATCAA;TAATCAA) 0 common in clinvar


Make rs397509134(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091463
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509134
dbSNP (old)rs397509134
ClinGenrs397509134
ebirs397509134
HLIrs397509134
Exacrs397509134
Gnomadrs397509134
Varsomers397509134
Maprs397509134
PheGenIrs397509134
Biobankrs397509134
1000 genomesrs397509134
hgdprs397509134
ensemblrs397509134
gopubmedrs397509134
geneviewrs397509134
scholarrs397509134
googlers397509134
pharmgkbrs397509134
gwascentralrs397509134
openSNPrs397509134
23andMers397509134
23andMe allrs397509134
SNP Nexus

SNPshotrs397509134
SNPdbers397509134
MSV3drs397509134
GWAS Ctlgrs397509134
Max Magnitude6
ClinVar
Risk rs397509134(-;-)
Alt rs397509134(-;-)
Reference Rs397509134(TAATCAA;TAATCAA)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41243480_41243486delTTGATTA
CLNSRC ClinVar
CLNACC RCV000048429.2, RCV000257056.2,