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rs869320675

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869320675(A;A)
Make rs869320675(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position1887487
GeneMYT1L
is asnp
is mentioned by
dbSNPrs869320675
ebirs869320675
HLIrs869320675
Exacrs869320675
Varsomers869320675
Maprs869320675
PheGenIrs869320675
hapmaprs869320675
1000 genomesrs869320675
hgdprs869320675
ensemblrs869320675
gopubmedrs869320675
geneviewrs869320675
scholarrs869320675
googlers869320675
pharmgkbrs869320675
gwascentralrs869320675
openSNPrs869320675
23andMers869320675
23andMe allrs869320675
SNP Nexus

SNPshotrs869320675
SNPdbers869320675
MSV3drs869320675
GWAS Ctlgrs869320675
Max Magnitude0
ClinVar
Risk rs869320675(A;A)
Alt rs869320675(A;A)
Reference rs869320675(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene MYT1L
CLNDBN Mental retardation, autosomal dominant 39
Reversed 1
HGVS NC_000002.11:g.1891259C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000190461.2,