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rs1057521913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521913(C;C)
Make rs1057521913(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position76733378
GeneMETTL23
is asnp
is mentioned by
dbSNPrs1057521913
dbSNP (old)rs1057521913
ClinGenrs1057521913
ebirs1057521913
HLIrs1057521913
Exacrs1057521913
Gnomadrs1057521913
Varsomers1057521913
LitVarrs1057521913
Maprs1057521913
PheGenIrs1057521913
Biobankrs1057521913
1000 genomesrs1057521913
hgdprs1057521913
ensemblrs1057521913
gopubmedrs1057521913
geneviewrs1057521913
scholarrs1057521913
googlers1057521913
pharmgkbrs1057521913
gwascentralrs1057521913
openSNPrs1057521913
23andMers1057521913
23andMe allrs1057521913
SNPshotrs1057521913
SNPdbers1057521913
MSV3drs1057521913
GWAS Ctlgrs1057521913
Max Magnitude0
ClinVar
Risk rs1057521913(C;C)
Alt rs1057521913(C;C)
Reference Rs1057521913(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene METTL23
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.74729460G>C
CLNSRC
CLNACC RCV000421646.1,