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rs1064794713

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position1917240
GeneMYT1L
is asnp
is mentioned by
dbSNPrs1064794713
dbSNP (old)rs1064794713
ClinGenrs1064794713
ebirs1064794713
HLIrs1064794713
Exacrs1064794713
Gnomadrs1064794713
Varsomers1064794713
Maprs1064794713
PheGenIrs1064794713
Biobankrs1064794713
1000 genomesrs1064794713
hgdprs1064794713
ensemblrs1064794713
gopubmedrs1064794713
geneviewrs1064794713
scholarrs1064794713
googlers1064794713
pharmgkbrs1064794713
gwascentralrs1064794713
openSNPrs1064794713
23andMers1064794713
23andMe allrs1064794713
SNPshotrs1064794713
SNPdbers1064794713
MSV3drs1064794713
GWAS Ctlgrs1064794713
Max Magnitude0
ClinVar
Risk rs1064794713(T;T)
Alt rs1064794713(T;T)
Reference Rs1064794713(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYT1L
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.1921012G>A
CLNSRC
CLNACC RCV000483053.1,