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

rs397509292

From SNPedia

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
ebirs397509292
HLIrs397509292
Exacrs397509292
Varsomers397509292
Maprs397509292
PheGenIrs397509292
hapmaprs397509292
1000 genomesrs397509292
hgdprs397509292
ensemblrs397509292
gopubmedrs397509292
geneviewrs397509292
scholarrs397509292
googlers397509292
pharmgkbrs397509292
gwascentralrs397509292
openSNPrs397509292
23andMers397509292
23andMe allrs397509292
SNP Nexus

SNPshotrs397509292
SNPdbers397509292
MSV3drs397509292
GWAS Ctlgrs397509292
Max Magnitude0
ClinVar
Risk rs397509292(;)
Alt rs397509292(;)
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, RCV000112690.1,