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rs878853045

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853045(A;A)
Make rs878853045(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position1912023
GeneMYT1L
is asnp
is mentioned by
dbSNPrs878853045
ebirs878853045
HLIrs878853045
Exacrs878853045
Varsomers878853045
Maprs878853045
PheGenIrs878853045
hapmaprs878853045
1000 genomesrs878853045
hgdprs878853045
ensemblrs878853045
gopubmedrs878853045
geneviewrs878853045
scholarrs878853045
googlers878853045
pharmgkbrs878853045
gwascentralrs878853045
openSNPrs878853045
23andMers878853045
23andMe allrs878853045
SNP Nexus

SNPshotrs878853045
SNPdbers878853045
MSV3drs878853045
GWAS Ctlgrs878853045
Max Magnitude0
ClinVar
Risk rs878853045(A;A)
Alt rs878853045(A;A)
Reference rs878853045(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYT1L
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.1915795C>T
CLNSRC
CLNACC RCV000224698.1,