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rs397509179

From SNPedia

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


Make rs397509179(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43076516
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509179
dbSNP (classic)rs397509179
ClinGenrs397509179
ebirs397509179
HLIrs397509179
Exacrs397509179
Gnomadrs397509179
Varsomers397509179
LitVarrs397509179
Maprs397509179
PheGenIrs397509179
Biobankrs397509179
1000 genomesrs397509179
hgdprs397509179
ensemblrs397509179
geneviewrs397509179
scholarrs397509179
googlers397509179
pharmgkbrs397509179
gwascentralrs397509179
openSNPrs397509179
23andMers397509179
SNPshotrs397509179
SNPdbers397509179
MSV3drs397509179
GWAS Ctlgrs397509179
Max Magnitude6
ClinVar
Risk rs397509179(-;-)
Alt rs397509179(-;-)
Reference Rs397509179(A;A)
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.41228533delT
CLNSRC ClinVar
CLNACC RCV000048564.2, RCV000256861.2,