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rs397509294

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509294(-;-)
Make rs397509294(-;T)
Make rs397509294(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045736
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509294
ebirs397509294
HLIrs397509294
Exacrs397509294
Varsomers397509294
Maprs397509294
PheGenIrs397509294
hapmaprs397509294
1000 genomesrs397509294
hgdprs397509294
ensemblrs397509294
gopubmedrs397509294
geneviewrs397509294
scholarrs397509294
googlers397509294
pharmgkbrs397509294
gwascentralrs397509294
openSNPrs397509294
23andMers397509294
23andMe allrs397509294
SNP Nexus

SNPshotrs397509294
SNPdbers397509294
MSV3drs397509294
GWAS Ctlgrs397509294
Max Magnitude0
ClinVar
Risk rs397509294(T;T)
Alt rs397509294(T;T)
Reference rs397509294(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41197754dupA
CLNSRC ClinVar
CLNACC RCV000049040.2,