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rs11567847

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs11567847(C;C)
Make rs11567847(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position12937202
GeneTEAD1
is asnp
is mentioned by
dbSNPrs11567847
ebirs11567847
HLIrs11567847
Exacrs11567847
Varsomers11567847
Maprs11567847
PheGenIrs11567847
hapmaprs11567847
1000 genomesrs11567847
hgdprs11567847
ensemblrs11567847
gopubmedrs11567847
geneviewrs11567847
scholarrs11567847
googlers11567847
pharmgkbrs11567847
gwascentralrs11567847
openSNPrs11567847
23andMers11567847
23andMe allrs11567847
SNP Nexus

SNPshotrs11567847
SNPdbers11567847
MSV3drs11567847
GWAS Ctlgrs11567847
Max Magnitude0
? (C;C) (C;T) (T;T) 28
OMIM189967
Desc
Variant0001
Relatedalso


ClinVar
Risk rs11567847(C;C)
Alt rs11567847(C;C)
Reference rs11567847(T;T)
Significance Pathogenic
Disease Sveinsson choreoretinal atrophy
Variation info
Gene TEAD1
CLNDBN Sveinsson choreoretinal atrophy
Reversed 0
HGVS NC_000011.9:g.12958749T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013465.23,