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rs1057524822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524822(C;G)
Make rs1057524822(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position46337942
GeneTRMU
is asnp
is mentioned by
dbSNPrs1057524822
dbSNP (classic)rs1057524822
ClinGenrs1057524822
ebirs1057524822
HLIrs1057524822
Exacrs1057524822
Gnomadrs1057524822
Varsomers1057524822
LitVarrs1057524822
Maprs1057524822
PheGenIrs1057524822
Biobankrs1057524822
1000 genomesrs1057524822
hgdprs1057524822
ensemblrs1057524822
geneviewrs1057524822
scholarrs1057524822
googlers1057524822
pharmgkbrs1057524822
gwascentralrs1057524822
openSNPrs1057524822
23andMers1057524822
23andMe allrs1057524822
SNPshotrs1057524822
SNPdbers1057524822
MSV3drs1057524822
GWAS Ctlgrs1057524822
Max Magnitude0
ClinVar
Risk rs1057524822(G;G)
Alt rs1057524822(G;G)
Reference Rs1057524822(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TRMU
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.46733839C>G
CLNSRC
CLNACC RCV000424646.1,