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rs397509273

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509273(-;-)
Make rs397509273(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43099786
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509273
ebirs397509273
HLIrs397509273
Exacrs397509273
Varsomers397509273
Maprs397509273
PheGenIrs397509273
hapmaprs397509273
1000 genomesrs397509273
hgdprs397509273
ensemblrs397509273
gopubmedrs397509273
geneviewrs397509273
scholarrs397509273
googlers397509273
pharmgkbrs397509273
gwascentralrs397509273
openSNPrs397509273
23andMers397509273
23andMe allrs397509273
SNP Nexus

SNPshotrs397509273
SNPdbers397509273
MSV3drs397509273
GWAS Ctlgrs397509273
Max Magnitude0
ClinVar
Risk rs397509273(;)
Alt rs397509273(;)
Reference rs397509273(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41251803delT
CLNSRC ClinVar
CLNACC RCV000048966.2,