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rs1057519560

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519560(C;C)
Make rs1057519560(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position1917264
GeneMYT1L
is asnp
is mentioned by
dbSNPrs1057519560
dbSNP (old)rs1057519560
ClinGenrs1057519560
ebirs1057519560
HLIrs1057519560
Exacrs1057519560
Gnomadrs1057519560
Varsomers1057519560
Maprs1057519560
PheGenIrs1057519560
Biobankrs1057519560
1000 genomesrs1057519560
hgdprs1057519560
ensemblrs1057519560
gopubmedrs1057519560
geneviewrs1057519560
scholarrs1057519560
googlers1057519560
pharmgkbrs1057519560
gwascentralrs1057519560
openSNPrs1057519560
23andMers1057519560
23andMe allrs1057519560
SNPshotrs1057519560
SNPdbers1057519560
MSV3drs1057519560
GWAS Ctlgrs1057519560
Max Magnitude0
ClinVar
Risk rs1057519560(C;C)
Alt rs1057519560(C;C)
Reference Rs1057519560(T;T)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene MYT1L
CLNDBN Mental retardation, autosomal dominant 39
Reversed 1
HGVS NC_000002.11:g.1921036A>G
CLNSRC
CLNACC RCV000416999.1,