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rs397509241

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509241(-;-)
Make rs397509241(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43057098
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509241
ebirs397509241
HLIrs397509241
Exacrs397509241
Varsomers397509241
Maprs397509241
PheGenIrs397509241
hapmaprs397509241
1000 genomesrs397509241
hgdprs397509241
ensemblrs397509241
gopubmedrs397509241
geneviewrs397509241
scholarrs397509241
googlers397509241
pharmgkbrs397509241
gwascentralrs397509241
openSNPrs397509241
23andMers397509241
23andMe allrs397509241
SNP Nexus

SNPshotrs397509241
SNPdbers397509241
MSV3drs397509241
GWAS Ctlgrs397509241
Max Magnitude0
ClinVar
Risk rs397509241(;)
Alt rs397509241(;)
Reference rs397509241(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.41209115delC
CLNSRC ClinVar
CLNACC RCV000048873.2,