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rs397509278

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509278(A;T)
Make rs397509278(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43049118
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509278
ebirs397509278
HLIrs397509278
Exacrs397509278
Varsomers397509278
Maprs397509278
PheGenIrs397509278
hapmaprs397509278
1000 genomesrs397509278
hgdprs397509278
ensemblrs397509278
gopubmedrs397509278
geneviewrs397509278
scholarrs397509278
googlers397509278
pharmgkbrs397509278
gwascentralrs397509278
openSNPrs397509278
23andMers397509278
23andMe allrs397509278
SNP Nexus

SNPshotrs397509278
SNPdbers397509278
MSV3drs397509278
GWAS Ctlgrs397509278
Max Magnitude0
ClinVar
Risk rs397509278(T;T)
Alt rs397509278(T;T)
Reference rs397509278(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.41201135T>A
CLNSRC ClinVar
CLNACC RCV000048975.2,