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rs397509203

From SNPedia

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


Make rs397509203(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43071008
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509203
ClinGenrs397509203
ebirs397509203
HLIrs397509203
Exacrs397509203
Varsomers397509203
Maprs397509203
PheGenIrs397509203
hapmaprs397509203
1000 genomesrs397509203
hgdprs397509203
ensemblrs397509203
gopubmedrs397509203
geneviewrs397509203
scholarrs397509203
googlers397509203
pharmgkbrs397509203
gwascentralrs397509203
openSNPrs397509203
23andMers397509203
23andMe allrs397509203
SNP Nexus

SNPshotrs397509203
SNPdbers397509203
MSV3drs397509203
GWAS Ctlgrs397509203
Max Magnitude6
ClinVar
Risk rs397509203(-;-)
Alt rs397509203(-;-)
Reference Rs397509203(GA;GA)
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.41223025_41223026delTC
CLNSRC ClinVar
CLNACC RCV000048689.2, RCV000256921.2,