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rs397509064

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509064(-;-)
Make rs397509064(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092115
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509064
ebirs397509064
HLIrs397509064
Exacrs397509064
Varsomers397509064
Maprs397509064
PheGenIrs397509064
hapmaprs397509064
1000 genomesrs397509064
hgdprs397509064
ensemblrs397509064
gopubmedrs397509064
geneviewrs397509064
scholarrs397509064
googlers397509064
pharmgkbrs397509064
gwascentralrs397509064
openSNPrs397509064
23andMers397509064
23andMe allrs397509064
SNP Nexus

SNPshotrs397509064
SNPdbers397509064
MSV3drs397509064
GWAS Ctlgrs397509064
Max Magnitude0
ClinVar
Risk rs397509064(;)
Alt rs397509064(;)
Reference rs397509064(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.41244132delC
CLNSRC ClinVar
CLNACC RCV000048185.2,