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rs397509076

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397509076(-;-)
Make rs397509076(-;TT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092036
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509076
ebirs397509076
HLIrs397509076
Exacrs397509076
Varsomers397509076
Maprs397509076
PheGenIrs397509076
hapmaprs397509076
1000 genomesrs397509076
hgdprs397509076
ensemblrs397509076
gopubmedrs397509076
geneviewrs397509076
scholarrs397509076
googlers397509076
pharmgkbrs397509076
gwascentralrs397509076
openSNPrs397509076
23andMers397509076
23andMe allrs397509076
SNP Nexus

SNPshotrs397509076
SNPdbers397509076
MSV3drs397509076
GWAS Ctlgrs397509076
Max Magnitude0
ClinVar
Risk rs397509076(;)
Alt rs397509076(;)
Reference rs397509076(TT;TT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244053_41244054delAA
CLNSRC ClinVar
CLNACC RCV000048216.2,