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rs144037629

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs144037629(C;T)
Make rs144037629(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position223959667
GeneMRPL44
is asnp
is mentioned by
dbSNPrs144037629
ebirs144037629
HLIrs144037629
Exacrs144037629
Varsomers144037629
Maprs144037629
PheGenIrs144037629
hapmaprs144037629
1000 genomesrs144037629
hgdprs144037629
ensemblrs144037629
gopubmedrs144037629
geneviewrs144037629
scholarrs144037629
googlers144037629
pharmgkbrs144037629
gwascentralrs144037629
openSNPrs144037629
23andMers144037629
23andMe allrs144037629
SNP Nexus

SNPshotrs144037629
SNPdbers144037629
MSV3drs144037629
GWAS Ctlgrs144037629
Max Magnitude0
ClinVar
Risk rs144037629(T;T)
Alt rs144037629(T;T)
Reference rs144037629(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MRPL44
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.224824384C>T
CLNSRC
CLNACC RCV000196498.2,