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rs397509231

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509231(-;-)
Make rs397509231(-;T)
Make rs397509231(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position43063871
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509231
ebirs397509231
HLIrs397509231
Exacrs397509231
Varsomers397509231
Maprs397509231
PheGenIrs397509231
hapmaprs397509231
1000 genomesrs397509231
hgdprs397509231
ensemblrs397509231
gopubmedrs397509231
geneviewrs397509231
scholarrs397509231
googlers397509231
pharmgkbrs397509231
gwascentralrs397509231
openSNPrs397509231
23andMers397509231
23andMe allrs397509231
SNP Nexus

SNPshotrs397509231
SNPdbers397509231
MSV3drs397509231
GWAS Ctlgrs397509231
Max Magnitude0
ClinVar
Risk rs397509231(T;T)
Alt rs397509231(T;T)
Reference rs397509231(;)
Significance Probable-Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41215889dupA
CLNSRC ClinVar
CLNACC RCV000048821.3, RCV000083060.2,