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rs786204789

From SNPedia

Orientationminus
Geno Mag Summary
(GGTT;GGTT) 0 common in clinvar
Make rs786204789(-;-)
Make rs786204789(-;GGTT)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position165768250
GeneLOC100147773, TMCO1
is asnp
is mentioned by
dbSNPrs786204789
ebirs786204789
HLIrs786204789
Exacrs786204789
Varsomers786204789
Maprs786204789
PheGenIrs786204789
hapmaprs786204789
1000 genomesrs786204789
hgdprs786204789
ensemblrs786204789
gopubmedrs786204789
geneviewrs786204789
scholarrs786204789
googlers786204789
pharmgkbrs786204789
gwascentralrs786204789
openSNPrs786204789
23andMers786204789
23andMe allrs786204789
SNP Nexus

SNPshotrs786204789
SNPdbers786204789
MSV3drs786204789
GWAS Ctlgrs786204789
Max Magnitude0
ClinVar
Risk rs786204789(;)
Alt rs786204789(;)
Reference rs786204789(GGTT;GGTT)
Significance Pathogenic
Disease Craniofacial dysmorphism
Variation info
Gene LOC100147773 RP11-466F5.8 TMCO1
CLNDBN Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
Reversed 1
HGVS NC_000001.10:g.165737487_165737490delAACC
CLNSRC
CLNACC RCV000169680.1,