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rs397509067

From SNPedia

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


Make rs397509067(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092092
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509067
dbSNP (old)rs397509067
ClinGenrs397509067
ebirs397509067
HLIrs397509067
Exacrs397509067
Varsomers397509067
Maprs397509067
PheGenIrs397509067
Biobankrs397509067
1000 genomesrs397509067
hgdprs397509067
ensemblrs397509067
gopubmedrs397509067
geneviewrs397509067
scholarrs397509067
googlers397509067
pharmgkbrs397509067
gwascentralrs397509067
openSNPrs397509067
23andMers397509067
23andMe allrs397509067
SNP Nexus

SNPshotrs397509067
SNPdbers397509067
MSV3drs397509067
GWAS Ctlgrs397509067
Max Magnitude6
ClinVar
Risk rs397509067(-;-)
Alt rs397509067(-;-)
Reference Rs397509067(TGTT;TGTT)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer not specified Familial cancer of breast not provided
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1 not specified Familial cancer of breast not provided
Reversed 1
HGVS NC_000017.10:g.41244109_41244112delAACA
CLNSRC ClinVar
CLNACC RCV000048197.3, RCV000077549.4, RCV000239029.1, RCV000459696.1, RCV000478411.1,