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rs397509054

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509054(-;-)
Make rs397509054(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092217
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509054
ebirs397509054
HLIrs397509054
Exacrs397509054
Varsomers397509054
Maprs397509054
PheGenIrs397509054
hapmaprs397509054
1000 genomesrs397509054
hgdprs397509054
ensemblrs397509054
gopubmedrs397509054
geneviewrs397509054
scholarrs397509054
googlers397509054
pharmgkbrs397509054
gwascentralrs397509054
openSNPrs397509054
23andMers397509054
23andMe allrs397509054
SNP Nexus

SNPshotrs397509054
SNPdbers397509054
MSV3drs397509054
GWAS Ctlgrs397509054
Max Magnitude0
ClinVar
Risk rs397509054(;)
Alt rs397509054(;)
Reference rs397509054(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244234delT
CLNSRC ClinVar
CLNACC RCV000048140.2,