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rs397509204

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509204(-;-)
Make rs397509204(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43071004
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509204
ebirs397509204
HLIrs397509204
Exacrs397509204
Varsomers397509204
Maprs397509204
PheGenIrs397509204
hapmaprs397509204
1000 genomesrs397509204
hgdprs397509204
ensemblrs397509204
gopubmedrs397509204
geneviewrs397509204
scholarrs397509204
googlers397509204
pharmgkbrs397509204
gwascentralrs397509204
openSNPrs397509204
23andMers397509204
23andMe allrs397509204
SNP Nexus

SNPshotrs397509204
SNPdbers397509204
MSV3drs397509204
GWAS Ctlgrs397509204
Max Magnitude0
ClinVar
Risk rs397509204(;)
Alt rs397509204(;)
Reference rs397509204(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41223021delG
CLNSRC ClinVar
CLNACC RCV000048692.2,