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rs397509166

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGAAAAGTAGTGAATAC;AGAAAAGTAGTGAATAC) 0 common in clinvar
Make rs397509166(-;-)
Make rs397509166(-;AGAAAAGTAGTGAATAC)
ReferenceGRCh38 38.1/141
Chromosome17
Position43076583
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509166
ebirs397509166
HLIrs397509166
Exacrs397509166
Varsomers397509166
Maprs397509166
PheGenIrs397509166
hapmaprs397509166
1000 genomesrs397509166
hgdprs397509166
ensemblrs397509166
gopubmedrs397509166
geneviewrs397509166
scholarrs397509166
googlers397509166
pharmgkbrs397509166
gwascentralrs397509166
openSNPrs397509166
23andMers397509166
23andMe allrs397509166
SNP Nexus

SNPshotrs397509166
SNPdbers397509166
MSV3drs397509166
GWAS Ctlgrs397509166
Max Magnitude0
ClinVar
Risk rs397509166(;)
Alt rs397509166(;)
Reference rs397509166(AGAAAAGTAGTGAATAC;AGAAAAGTAGTGAATAC)
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.41228600_41228616del17
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048541.2, RCV000112329.1,