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rs1064793635

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position1922701
GeneMYT1L
is asnp
is mentioned by
dbSNPrs1064793635
dbSNP (classic)rs1064793635
ClinGenrs1064793635
ebirs1064793635
HLIrs1064793635
Exacrs1064793635
Gnomadrs1064793635
Varsomers1064793635
LitVarrs1064793635
Maprs1064793635
PheGenIrs1064793635
Biobankrs1064793635
1000 genomesrs1064793635
hgdprs1064793635
ensemblrs1064793635
geneviewrs1064793635
scholarrs1064793635
googlers1064793635
pharmgkbrs1064793635
gwascentralrs1064793635
openSNPrs1064793635
23andMers1064793635
23andMe allrs1064793635
SNPshotrs1064793635
SNPdbers1064793635
MSV3drs1064793635
GWAS Ctlgrs1064793635
Max Magnitude0
ClinVar
Risk rs1064793635(-;-)
Alt rs1064793635(-;-)
Reference Rs1064793635(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYT1L
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.1926473delG
CLNSRC
CLNACC RCV000479302.1,