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rs397509117

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509117(-;-)
Make rs397509117(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091621
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509117
ebirs397509117
HLIrs397509117
Exacrs397509117
Varsomers397509117
Maprs397509117
PheGenIrs397509117
hapmaprs397509117
1000 genomesrs397509117
hgdprs397509117
ensemblrs397509117
gopubmedrs397509117
geneviewrs397509117
scholarrs397509117
googlers397509117
pharmgkbrs397509117
gwascentralrs397509117
openSNPrs397509117
23andMers397509117
23andMe allrs397509117
SNP Nexus

SNPshotrs397509117
SNPdbers397509117
MSV3drs397509117
GWAS Ctlgrs397509117
Max Magnitude0
ClinVar
Risk rs397509117(;)
Alt rs397509117(;)
Reference rs397509117(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.41243638delC
CLNSRC ClinVar
CLNACC RCV000048377.2,