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rs863223919

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223919(A;A)
Make rs863223919(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position100989177
GeneC10orf2, MRPL43
is asnp
is mentioned by
dbSNPrs863223919
ebirs863223919
HLIrs863223919
Exacrs863223919
Varsomers863223919
Maprs863223919
PheGenIrs863223919
hapmaprs863223919
1000 genomesrs863223919
hgdprs863223919
ensemblrs863223919
gopubmedrs863223919
geneviewrs863223919
scholarrs863223919
googlers863223919
pharmgkbrs863223919
gwascentralrs863223919
openSNPrs863223919
23andMers863223919
23andMe allrs863223919
SNP Nexus

SNPshotrs863223919
SNPdbers863223919
MSV3drs863223919
GWAS Ctlgrs863223919
Max Magnitude0
ClinVar
Risk rs863223919(A;A)
Alt rs863223919(A;A)
Reference rs863223919(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MRPL43 C10orf2
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.102748934C>T
CLNSRC
CLNACC RCV000198844.1,