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rs397509087

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAAATT;GAAATT) 0 common in clinvar
Make rs397509087(AA;AA)
Make rs397509087(AA;GAAATT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091905
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509087
ebirs397509087
HLIrs397509087
Exacrs397509087
Varsomers397509087
Maprs397509087
PheGenIrs397509087
hapmaprs397509087
1000 genomesrs397509087
hgdprs397509087
ensemblrs397509087
gopubmedrs397509087
geneviewrs397509087
scholarrs397509087
googlers397509087
pharmgkbrs397509087
gwascentralrs397509087
openSNPrs397509087
23andMers397509087
23andMe allrs397509087
SNP Nexus

SNPshotrs397509087
SNPdbers397509087
MSV3drs397509087
GWAS Ctlgrs397509087
Max Magnitude0
ClinVar
Risk rs397509087(AA;AA)
Alt rs397509087(AA;AA)
Reference rs397509087(GAAATT;GAAATT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243922_41243927delAATTTCinsTT
CLNSRC ClinVar
CLNACC RCV000048257.2,