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rs397509145

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509145(-;-)
Make rs397509145(-;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43090962
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509145
ClinGenrs397509145
ebirs397509145
HLIrs397509145
Exacrs397509145
Varsomers397509145
Maprs397509145
PheGenIrs397509145
hapmaprs397509145
1000 genomesrs397509145
hgdprs397509145
ensemblrs397509145
gopubmedrs397509145
geneviewrs397509145
scholarrs397509145
googlers397509145
pharmgkbrs397509145
gwascentralrs397509145
openSNPrs397509145
23andMers397509145
23andMe allrs397509145
SNP Nexus

SNPshotrs397509145
SNPdbers397509145
MSV3drs397509145
GWAS Ctlgrs397509145
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397509145(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41242979delA
CLNSRC ClinVar
CLNACC RCV000048468.2,