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rs397509041

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509041(-;-)
Make rs397509041(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092374
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509041
ebirs397509041
HLIrs397509041
Exacrs397509041
Varsomers397509041
Maprs397509041
PheGenIrs397509041
hapmaprs397509041
1000 genomesrs397509041
hgdprs397509041
ensemblrs397509041
gopubmedrs397509041
geneviewrs397509041
scholarrs397509041
googlers397509041
pharmgkbrs397509041
gwascentralrs397509041
openSNPrs397509041
23andMers397509041
23andMe allrs397509041
SNP Nexus

SNPshotrs397509041
SNPdbers397509041
MSV3drs397509041
GWAS Ctlgrs397509041
Max Magnitude0
ClinVar
Risk rs397509041(;)
Alt rs397509041(;)
Reference rs397509041(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.41244391delC
CLNSRC ClinVar
CLNACC RCV000048086.2,