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rs397509290

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GTGACCCGAG;GTGACCCGAG) 0 common in clinvar
Make rs397509290(-;-)
Make rs397509290(-;GTGACCCGAG)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045764
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509290
ebirs397509290
HLIrs397509290
Exacrs397509290
Varsomers397509290
Maprs397509290
PheGenIrs397509290
hapmaprs397509290
1000 genomesrs397509290
hgdprs397509290
ensemblrs397509290
gopubmedrs397509290
geneviewrs397509290
scholarrs397509290
googlers397509290
pharmgkbrs397509290
gwascentralrs397509290
openSNPrs397509290
23andMers397509290
23andMe allrs397509290
SNP Nexus

SNPshotrs397509290
SNPdbers397509290
MSV3drs397509290
GWAS Ctlgrs397509290
Max Magnitude0
ClinVar
Risk rs397509290(;)
Alt rs397509290(;)
Reference rs397509290(GTGACCCGAG;GTGACCCGAG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41197781_41197790delCTCGGGTCAC
CLNSRC ClinVar
CLNACC RCV000049018.2,