Have questions? Visit https://www.reddit.com/r/SNPedia

rs397509031

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ACTAAATGTAAGAAAAA;ACTAAATGTAAGAAAAA) 0 common in clinvar
Make rs397509031(-;-)
Make rs397509031(-;ACTAAATGTAAGAAAAA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092541
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509031
dbSNP (classic)rs397509031
ClinGenrs397509031
ebirs397509031
HLIrs397509031
Exacrs397509031
Gnomadrs397509031
Varsomers397509031
LitVarrs397509031
Maprs397509031
PheGenIrs397509031
Biobankrs397509031
1000 genomesrs397509031
hgdprs397509031
ensemblrs397509031
geneviewrs397509031
scholarrs397509031
googlers397509031
pharmgkbrs397509031
gwascentralrs397509031
openSNPrs397509031
23andMers397509031
SNPshotrs397509031
SNPdbers397509031
MSV3drs397509031
GWAS Ctlgrs397509031
Max Magnitude0
ClinVar
Risk rs397509031(-;-)
Alt rs397509031(-;-)
Reference Rs397509031(ACTAAATGTAAGAAAAA;ACTAAATGTAAGAAAAA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244558_41244574del17
CLNSRC ClinVar
CLNACC RCV000048028.2,