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rs869320676

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869320676(G;G)
Make rs869320676(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position1903189
GeneMYT1L
is asnp
is mentioned by
dbSNPrs869320676
ebirs869320676
HLIrs869320676
Exacrs869320676
Varsomers869320676
Maprs869320676
PheGenIrs869320676
hapmaprs869320676
1000 genomesrs869320676
hgdprs869320676
ensemblrs869320676
gopubmedrs869320676
geneviewrs869320676
scholarrs869320676
googlers869320676
pharmgkbrs869320676
gwascentralrs869320676
openSNPrs869320676
23andMers869320676
23andMe allrs869320676
SNP Nexus

SNPshotrs869320676
SNPdbers869320676
MSV3drs869320676
GWAS Ctlgrs869320676
Max Magnitude0
ClinVar
Risk rs869320676(G;G)
Alt rs869320676(G;G)
Reference rs869320676(T;T)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene MYT1L
CLNDBN Mental retardation, autosomal dominant 39
Reversed 1
HGVS NC_000002.11:g.1906961A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000190462.2,