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rs587777645

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGAT;AAGAT) 0 common in clinvar
Make rs587777645(-;-)
Make rs587777645(-;AGATA)
Make rs587777645(AGATA;AGATA)
ReferenceGRCh38 38.1/142
Chromosome17
Position76733175
GeneMETTL23
is asnp
is mentioned by
dbSNPrs587777645
ebirs587777645
HLIrs587777645
Exacrs587777645
Varsomers587777645
Maprs587777645
PheGenIrs587777645
hapmaprs587777645
1000 genomesrs587777645
hgdprs587777645
ensemblrs587777645
gopubmedrs587777645
geneviewrs587777645
scholarrs587777645
googlers587777645
pharmgkbrs587777645
gwascentralrs587777645
openSNPrs587777645
23andMers587777645
23andMe allrs587777645
SNP Nexus

SNPshotrs587777645
SNPdbers587777645
MSV3drs587777645
GWAS Ctlgrs587777645
Max Magnitude0
ClinVar
Risk rs587777645(;)
Alt rs587777645(;)
Reference rs587777645(AAGAT;AAGAT)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene METTL23
CLNDBN Mental retardation, autosomal recessive 44
Reversed 0
HGVS NC_000017.10:g.74729257_74729261delAGATA
CLNSRC OMIM Allelic Variant
CLNACC RCV000133533.3,