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rs397509292

From SNPedia

Merged intors80357839
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509292(-;-)
Make rs397509292(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045758
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509292
dbSNP (classic)rs397509292
ClinGenrs397509292
ebirs397509292
HLIrs397509292
Exacrs397509292
Gnomadrs397509292
Varsomers397509292
LitVarrs397509292
Maprs397509292
PheGenIrs397509292
Biobankrs397509292
1000 genomesrs397509292
hgdprs397509292
ensemblrs397509292
geneviewrs397509292
scholarrs397509292
googlers397509292
pharmgkbrs397509292
gwascentralrs397509292
openSNPrs397509292
23andMers397509292
SNPshotrs397509292
SNPdbers397509292
MSV3drs397509292
GWAS Ctlgrs397509292
StatusMerged into rs80357839
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397509292(G;G)
Significance Pathogenic
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.41197775delC
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000049031.2, RCV000112690.2,