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rs397509084

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509084(-;-)
Make rs397509084(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091948
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509084
ebirs397509084
HLIrs397509084
Exacrs397509084
Varsomers397509084
Maprs397509084
PheGenIrs397509084
hapmaprs397509084
1000 genomesrs397509084
hgdprs397509084
ensemblrs397509084
gopubmedrs397509084
geneviewrs397509084
scholarrs397509084
googlers397509084
pharmgkbrs397509084
gwascentralrs397509084
openSNPrs397509084
23andMers397509084
23andMe allrs397509084
SNP Nexus

SNPshotrs397509084
SNPdbers397509084
MSV3drs397509084
GWAS Ctlgrs397509084
Max Magnitude0
ClinVar
Risk rs397509084(;)
Alt rs397509084(;)
Reference rs397509084(C;C)
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.41243965delG
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048239.2, RCV000112123.1,