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rs397509191

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509191(-;-)
Make rs397509191(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43071190
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509191
ebirs397509191
HLIrs397509191
Exacrs397509191
Varsomers397509191
Maprs397509191
PheGenIrs397509191
hapmaprs397509191
1000 genomesrs397509191
hgdprs397509191
ensemblrs397509191
gopubmedrs397509191
geneviewrs397509191
scholarrs397509191
googlers397509191
pharmgkbrs397509191
gwascentralrs397509191
openSNPrs397509191
23andMers397509191
23andMe allrs397509191
SNP Nexus

SNPshotrs397509191
SNPdbers397509191
MSV3drs397509191
GWAS Ctlgrs397509191
Max Magnitude0
ClinVar
Risk rs397509191(;)
Alt rs397509191(;)
Reference rs397509191(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.41223207delG
CLNSRC ClinVar
CLNACC RCV000048642.2,