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rs397509282

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509282(-;-)
Make rs397509282(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43047691
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509282
ebirs397509282
HLIrs397509282
Exacrs397509282
Varsomers397509282
Maprs397509282
PheGenIrs397509282
hapmaprs397509282
1000 genomesrs397509282
hgdprs397509282
ensemblrs397509282
gopubmedrs397509282
geneviewrs397509282
scholarrs397509282
googlers397509282
pharmgkbrs397509282
gwascentralrs397509282
openSNPrs397509282
23andMers397509282
23andMe allrs397509282
SNP Nexus

SNPshotrs397509282
SNPdbers397509282
MSV3drs397509282
GWAS Ctlgrs397509282
Max Magnitude0
ClinVar
Risk rs397509282(;)
Alt rs397509282(;)
Reference rs397509282(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.41199708delT
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048986.2, RCV000112649.1,