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rs397509058

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGAA;AGAA) 0 common in clinvar
Make rs397509058(-;-)
Make rs397509058(-;AGAA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092186
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509058
ebirs397509058
HLIrs397509058
Exacrs397509058
Varsomers397509058
Maprs397509058
PheGenIrs397509058
hapmaprs397509058
1000 genomesrs397509058
hgdprs397509058
ensemblrs397509058
gopubmedrs397509058
geneviewrs397509058
scholarrs397509058
googlers397509058
pharmgkbrs397509058
gwascentralrs397509058
openSNPrs397509058
23andMers397509058
23andMe allrs397509058
SNP Nexus

SNPshotrs397509058
SNPdbers397509058
MSV3drs397509058
GWAS Ctlgrs397509058
Max Magnitude0
ClinVar
Risk rs397509058(;)
Alt rs397509058(;)
Reference rs397509058(AGAA;AGAA)
Significance Other
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41244203_41244206delTTCT
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048156.2, RCV000077543.4,