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rs397509167

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509167(A;A)
Make rs397509167(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43076593
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509167
ebirs397509167
HLIrs397509167
Exacrs397509167
Varsomers397509167
Maprs397509167
PheGenIrs397509167
hapmaprs397509167
1000 genomesrs397509167
hgdprs397509167
ensemblrs397509167
gopubmedrs397509167
geneviewrs397509167
scholarrs397509167
googlers397509167
pharmgkbrs397509167
gwascentralrs397509167
openSNPrs397509167
23andMers397509167
23andMe allrs397509167
SNP Nexus

SNPshotrs397509167
SNPdbers397509167
MSV3drs397509167
GWAS Ctlgrs397509167
Max Magnitude0
ClinVar
Risk rs397509167(A;A)
Alt rs397509167(A;A)
Reference rs397509167(G;G)
Significance Untested
Disease Familial cancer of breast not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.41228610C>T
CLNSRC ClinVar
CLNACC RCV000048542.2, RCV000174570.1, RCV000213599.1,