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rs397509263

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509263(-;-)
Make rs397509263(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43051062
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509263
ebirs397509263
HLIrs397509263
Exacrs397509263
Varsomers397509263
Maprs397509263
PheGenIrs397509263
hapmaprs397509263
1000 genomesrs397509263
hgdprs397509263
ensemblrs397509263
gopubmedrs397509263
geneviewrs397509263
scholarrs397509263
googlers397509263
pharmgkbrs397509263
gwascentralrs397509263
openSNPrs397509263
23andMers397509263
23andMe allrs397509263
SNP Nexus

SNPshotrs397509263
SNPdbers397509263
MSV3drs397509263
GWAS Ctlgrs397509263
Max Magnitude0
ClinVar
Risk rs397509263(;)
Alt rs397509263(;)
Reference rs397509263(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41203079delC
CLNSRC ClinVar
CLNACC RCV000048935.2,