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rs397508853

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508853(-;-)
Make rs397508853(-;T)
Make rs397508853(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094211
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508853
ebirs397508853
HLIrs397508853
Exacrs397508853
Varsomers397508853
Maprs397508853
PheGenIrs397508853
hapmaprs397508853
1000 genomesrs397508853
hgdprs397508853
ensemblrs397508853
gopubmedrs397508853
geneviewrs397508853
scholarrs397508853
googlers397508853
pharmgkbrs397508853
gwascentralrs397508853
openSNPrs397508853
23andMers397508853
23andMe allrs397508853
SNP Nexus

SNPshotrs397508853
SNPdbers397508853
MSV3drs397508853
GWAS Ctlgrs397508853
Max Magnitude0
ClinVar
Risk rs397508853(T;T)
Alt rs397508853(T;T)
Reference rs397508853(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246229dupA
CLNSRC ClinVar
CLNACC RCV000047416.2,