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rs1064793449

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Chromosome2
Position1922547
GeneMYT1L
is asnp
is mentioned by
dbSNPrs1064793449
dbSNP (old)rs1064793449
ClinGenrs1064793449
ebirs1064793449
HLIrs1064793449
Exacrs1064793449
Gnomadrs1064793449
Varsomers1064793449
Maprs1064793449
PheGenIrs1064793449
Biobankrs1064793449
1000 genomesrs1064793449
hgdprs1064793449
ensemblrs1064793449
gopubmedrs1064793449
geneviewrs1064793449
scholarrs1064793449
googlers1064793449
pharmgkbrs1064793449
gwascentralrs1064793449
openSNPrs1064793449
23andMers1064793449
23andMe allrs1064793449
SNPshotrs1064793449
SNPdbers1064793449
MSV3drs1064793449
GWAS Ctlgrs1064793449
Max Magnitude0
ClinVar
Risk rs1064793449(T;T)
Alt rs1064793449(T;T)
Reference Rs1064793449(GC;GC)
Significance Pathogenic
Disease not provided
Variation info
Gene MYT1L
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.1926319_1926320delGCinsA
CLNSRC
CLNACC RCV000483472.1,