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rs863223920

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223920(C;C)
Make rs863223920(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position100989320
GeneC10orf2, MRPL43
is asnp
is mentioned by
dbSNPrs863223920
ebirs863223920
HLIrs863223920
Exacrs863223920
Varsomers863223920
Maprs863223920
PheGenIrs863223920
hapmaprs863223920
1000 genomesrs863223920
hgdprs863223920
ensemblrs863223920
gopubmedrs863223920
geneviewrs863223920
scholarrs863223920
googlers863223920
pharmgkbrs863223920
gwascentralrs863223920
openSNPrs863223920
23andMers863223920
23andMe allrs863223920
SNP Nexus

SNPshotrs863223920
SNPdbers863223920
MSV3drs863223920
GWAS Ctlgrs863223920
Max Magnitude0
ClinVar
Risk rs863223920(C;C)
Alt rs863223920(C;C)
Reference rs863223920(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MRPL43 C10orf2
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.102749077C>G
CLNSRC
CLNACC RCV000195885.1,