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rs397509165

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509165(-;-)
Make rs397509165(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43082403
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509165
ebirs397509165
HLIrs397509165
Exacrs397509165
Varsomers397509165
Maprs397509165
PheGenIrs397509165
hapmaprs397509165
1000 genomesrs397509165
hgdprs397509165
ensemblrs397509165
gopubmedrs397509165
geneviewrs397509165
scholarrs397509165
googlers397509165
pharmgkbrs397509165
gwascentralrs397509165
openSNPrs397509165
23andMers397509165
23andMe allrs397509165
SNP Nexus

SNPshotrs397509165
SNPdbers397509165
MSV3drs397509165
GWAS Ctlgrs397509165
Max Magnitude0
ClinVar
Risk rs397509165(;)
Alt rs397509165(;)
Reference rs397509165(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.41234420delC
CLNSRC ClinVar
CLNACC RCV000048535.2,