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rs544369132

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs544369132(C;T)
Make rs544369132(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position139348322
GeneMRPS22
is asnp
is mentioned by
dbSNPrs544369132
ebirs544369132
HLIrs544369132
Exacrs544369132
Varsomers544369132
Maprs544369132
PheGenIrs544369132
hapmaprs544369132
1000 genomesrs544369132
hgdprs544369132
ensemblrs544369132
gopubmedrs544369132
geneviewrs544369132
scholarrs544369132
googlers544369132
pharmgkbrs544369132
gwascentralrs544369132
openSNPrs544369132
23andMers544369132
23andMe allrs544369132
SNP Nexus

SNPshotrs544369132
SNPdbers544369132
MSV3drs544369132
GWAS Ctlgrs544369132
Max Magnitude0
ClinVar
Risk rs544369132(T;T)
Alt rs544369132(T;T)
Reference rs544369132(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MRPS22
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.139067164C>T
CLNSRC
CLNACC RCV000196283.1,