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rs397509225

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTG;CTG) 0 common in clinvar
Make rs397509225(-;-)
Make rs397509225(-;CTG)
ReferenceGRCh38 38.1/141
Chromosome17
Position43063946
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509225
ebirs397509225
HLIrs397509225
Exacrs397509225
Varsomers397509225
Maprs397509225
PheGenIrs397509225
hapmaprs397509225
1000 genomesrs397509225
hgdprs397509225
ensemblrs397509225
gopubmedrs397509225
geneviewrs397509225
scholarrs397509225
googlers397509225
pharmgkbrs397509225
gwascentralrs397509225
openSNPrs397509225
23andMers397509225
23andMe allrs397509225
SNP Nexus

SNPshotrs397509225
SNPdbers397509225
MSV3drs397509225
GWAS Ctlgrs397509225
Max Magnitude0
ClinVar
Risk rs397509225(;)
Alt rs397509225(;)
Reference rs397509225(CTG;CTG)
Significance Probable-Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000017.10:g.41215963_41215965delCAG
CLNSRC ClinVar
CLNACC RCV000048779.2, RCV000083215.3, RCV000166817.1, RCV000237025.1,