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rs397509024

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509024(-;-)
Make rs397509024(-;T)
Make rs397509024(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092609
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509024
ebirs397509024
HLIrs397509024
Exacrs397509024
Varsomers397509024
Maprs397509024
PheGenIrs397509024
hapmaprs397509024
1000 genomesrs397509024
hgdprs397509024
ensemblrs397509024
gopubmedrs397509024
geneviewrs397509024
scholarrs397509024
googlers397509024
pharmgkbrs397509024
gwascentralrs397509024
openSNPrs397509024
23andMers397509024
23andMe allrs397509024
SNP Nexus

SNPshotrs397509024
SNPdbers397509024
MSV3drs397509024
GWAS Ctlgrs397509024
Max Magnitude0
ClinVar
Risk rs397509024(T;T)
Alt rs397509024(T;T)
Reference rs397509024(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244627dupA
CLNSRC ClinVar
CLNACC RCV000048012.2,