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rs863223921

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223921(C;C)
Make rs863223921(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position100989406
GeneC10orf2, MRPL43
is asnp
is mentioned by
dbSNPrs863223921
ebirs863223921
HLIrs863223921
Exacrs863223921
Varsomers863223921
Maprs863223921
PheGenIrs863223921
hapmaprs863223921
1000 genomesrs863223921
hgdprs863223921
ensemblrs863223921
gopubmedrs863223921
geneviewrs863223921
scholarrs863223921
googlers863223921
pharmgkbrs863223921
gwascentralrs863223921
openSNPrs863223921
23andMers863223921
23andMe allrs863223921
SNP Nexus

SNPshotrs863223921
SNPdbers863223921
MSV3drs863223921
GWAS Ctlgrs863223921
Max Magnitude0
ClinVar
Risk rs863223921(C;C)
Alt rs863223921(C;C)
Reference rs863223921(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MRPL43 C10orf2
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.102749163A>G
CLNSRC
CLNACC RCV000199662.1,