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rs397509120

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TACA;TACA) 0 common in clinvar
Make rs397509120(-;-)
Make rs397509120(-;TACA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091601
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509120
ebirs397509120
HLIrs397509120
Exacrs397509120
Varsomers397509120
Maprs397509120
PheGenIrs397509120
hapmaprs397509120
1000 genomesrs397509120
hgdprs397509120
ensemblrs397509120
gopubmedrs397509120
geneviewrs397509120
scholarrs397509120
googlers397509120
pharmgkbrs397509120
gwascentralrs397509120
openSNPrs397509120
23andMers397509120
23andMe allrs397509120
SNP Nexus

SNPshotrs397509120
SNPdbers397509120
MSV3drs397509120
GWAS Ctlgrs397509120
Max Magnitude0
ClinVar
Risk rs397509120(;)
Alt rs397509120(;)
Reference rs397509120(TACA;TACA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243618_41243621delTGTA
CLNSRC ClinVar
CLNACC RCV000048382.2,