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rs587777743

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777743(A;A)
Make rs587777743(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position99557386
GeneTRMT10A
is asnp
is mentioned by
dbSNPrs587777743
ebirs587777743
HLIrs587777743
Exacrs587777743
Varsomers587777743
Maprs587777743
PheGenIrs587777743
hapmaprs587777743
1000 genomesrs587777743
hgdprs587777743
ensemblrs587777743
gopubmedrs587777743
geneviewrs587777743
scholarrs587777743
googlers587777743
pharmgkbrs587777743
gwascentralrs587777743
openSNPrs587777743
23andMers587777743
23andMe allrs587777743
SNP Nexus

SNPshotrs587777743
SNPdbers587777743
MSV3drs587777743
GWAS Ctlgrs587777743
Max Magnitude0
ClinVar
Risk rs587777743(A;A)
Alt rs587777743(A;A)
Reference rs587777743(G;G)
Significance Pathogenic
Disease Microcephaly
Variation info
Gene TRMT10A
CLNDBN Microcephaly, short stature, and impaired glucose metabolism 1
Reversed 0
HGVS NC_000004.11:g.100478543G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144247.2,