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rs397509078

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GACAT;GACAT) 0 common in clinvar
Make rs397509078(-;-)
Make rs397509078(-;GACAT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092022
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509078
ebirs397509078
HLIrs397509078
Exacrs397509078
Varsomers397509078
Maprs397509078
PheGenIrs397509078
hapmaprs397509078
1000 genomesrs397509078
hgdprs397509078
ensemblrs397509078
gopubmedrs397509078
geneviewrs397509078
scholarrs397509078
googlers397509078
pharmgkbrs397509078
gwascentralrs397509078
openSNPrs397509078
23andMers397509078
23andMe allrs397509078
SNP Nexus

SNPshotrs397509078
SNPdbers397509078
MSV3drs397509078
GWAS Ctlgrs397509078
Max Magnitude0
ClinVar
Risk rs397509078(;)
Alt rs397509078(;)
Reference rs397509078(GACAT;GACAT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244039_41244043delATGTC
CLNSRC ClinVar
CLNACC RCV000048219.2,