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rs397507236

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507236(-;-)
Make rs397507236(-;C)
Make rs397507236(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43099855
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397507236
ebirs397507236
HLIrs397507236
Exacrs397507236
Varsomers397507236
Maprs397507236
PheGenIrs397507236
hapmaprs397507236
1000 genomesrs397507236
hgdprs397507236
ensemblrs397507236
gopubmedrs397507236
geneviewrs397507236
scholarrs397507236
googlers397507236
pharmgkbrs397507236
gwascentralrs397507236
openSNPrs397507236
23andMers397507236
23andMe allrs397507236
SNP Nexus

SNPshotrs397507236
SNPdbers397507236
MSV3drs397507236
GWAS Ctlgrs397507236
Max Magnitude0
ClinVar
Risk rs397507236(C;C)
Alt rs397507236(C;C)
Reference rs397507236(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41251873dupG
CLNSRC ClinVar
CLNACC RCV000031183.3,