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rs587777744

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777744(C;T)
Make rs587777744(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position99553814
GeneTRMT10A
is asnp
is mentioned by
dbSNPrs587777744
dbSNP (old)rs587777744
ClinGenrs587777744
ebirs587777744
HLIrs587777744
Exacrs587777744
Varsomers587777744
Maprs587777744
PheGenIrs587777744
Biobankrs587777744
1000 genomesrs587777744
hgdprs587777744
ensemblrs587777744
gopubmedrs587777744
geneviewrs587777744
scholarrs587777744
googlers587777744
pharmgkbrs587777744
gwascentralrs587777744
openSNPrs587777744
23andMers587777744
23andMe allrs587777744
SNP Nexus

SNPshotrs587777744
SNPdbers587777744
MSV3drs587777744
GWAS Ctlgrs587777744
Max Magnitude0
ClinVar
Risk rs587777744(T;T)
Alt rs587777744(T;T)
Reference Rs587777744(C;C)
Significance Pathogenic
Disease Microcephaly
Variation info
Gene TRMT10A
CLNDBN Microcephaly, short stature, and impaired glucose metabolism 1
Reversed 0
HGVS NC_000004.11:g.100474971C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000144248.3,