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rs760933323

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs760933323(-;-)
Make rs760933323(-;TT)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position76733583
GeneMETTL23
is asnp
is mentioned by
dbSNPrs760933323
dbSNP (classic)rs760933323
ClinGenrs760933323
ebirs760933323
HLIrs760933323
Exacrs760933323
Gnomadrs760933323
Varsomers760933323
LitVarrs760933323
Maprs760933323
PheGenIrs760933323
Biobankrs760933323
1000 genomesrs760933323
hgdprs760933323
ensemblrs760933323
geneviewrs760933323
scholarrs760933323
googlers760933323
pharmgkbrs760933323
gwascentralrs760933323
openSNPrs760933323
23andMers760933323
SNPshotrs760933323
SNPdbers760933323
MSV3drs760933323
GWAS Ctlgrs760933323
Max Magnitude0
ClinVar
Risk rs760933323(-;-)
Alt rs760933323(-;-)
Reference Rs760933323(TT;TT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene METTL23
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.74729665_74729666delTT
CLNSRC
CLNACC RCV000486806.1,