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rs3830031

From SNPedia

Merged intors1263791
Orientationplus
Stabilizedplus
Make rs3830031(A;A)
Make rs3830031(A;T)
Make rs3830031(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position21501530
GeneMETTL3
is asnp
is mentioned by
dbSNPrs3830031
ebirs3830031
HLIrs3830031
Exacrs3830031
Varsomers3830031
Maprs3830031
PheGenIrs3830031
hapmaprs3830031
1000 genomesrs3830031
hgdprs3830031
ensemblrs3830031
gopubmedrs3830031
geneviewrs3830031
scholarrs3830031
googlers3830031
pharmgkbrs3830031
gwascentralrs3830031
openSNPrs3830031
23andMers3830031
23andMe allrs3830031
SNP Nexus

SNPshotrs3830031
SNPdbers3830031
MSV3drs3830031
GWAS Ctlgrs3830031
StatusMerged into rs1263791
Max Magnitude
? (A;A) (A;T) (T;T) 28

[PMID 20523082] Intronic single nucleotide polymorphisms of engrailed homeobox 2 modulate the disease vulnerability of autism in a han chinese population