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rs267607138

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607138(C;T)
Make rs267607138(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position92015729
GeneTRIP11
is asnp
is mentioned by
dbSNPrs267607138
ebirs267607138
HLIrs267607138
Exacrs267607138
Varsomers267607138
Maprs267607138
PheGenIrs267607138
hapmaprs267607138
1000 genomesrs267607138
hgdprs267607138
ensemblrs267607138
gopubmedrs267607138
geneviewrs267607138
scholarrs267607138
googlers267607138
pharmgkbrs267607138
gwascentralrs267607138
openSNPrs267607138
23andMers267607138
23andMe allrs267607138
SNP Nexus

SNPshotrs267607138
SNPdbers267607138
MSV3drs267607138
GWAS Ctlgrs267607138
Max Magnitude0
ClinVar
Risk rs267607138(A,T;A,T)
Alt rs267607138(A,T;A,T)
Reference rs267607138(C;C)
Significance Pathogenic
Disease Achondrogenesis
Variation info
Gene TRIP11
CLNDBN Achondrogenesis, type IA
Reversed 1
HGVS NC_000014.8:g.92482073G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005843.3,