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rs372701032

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs372701032(C;T)
Make rs372701032(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position165752099
GeneTMCO1
is asnp
is mentioned by
dbSNPrs372701032
ebirs372701032
HLIrs372701032
Exacrs372701032
Varsomers372701032
Maprs372701032
PheGenIrs372701032
hapmaprs372701032
1000 genomesrs372701032
hgdprs372701032
ensemblrs372701032
gopubmedrs372701032
geneviewrs372701032
scholarrs372701032
googlers372701032
pharmgkbrs372701032
gwascentralrs372701032
openSNPrs372701032
23andMers372701032
23andMe allrs372701032
SNP Nexus

SNPshotrs372701032
SNPdbers372701032
MSV3drs372701032
GWAS Ctlgrs372701032
Max Magnitude0
ClinVar
Risk rs372701032(T;T)
Alt rs372701032(T;T)
Reference rs372701032(C;C)
Significance Pathogenic
Disease Craniofacial dysmorphism
Variation info
Gene TMCO1
CLNDBN Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
Reversed 0
HGVS NC_000001.10:g.165721336C>G
CLNSRC Baylor College of Medicine
CLNACC RCV000203247.1,