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rs863223917

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223917(C;G)
Make rs863223917(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position100988548
GeneC10orf2, MRPL43
is asnp
is mentioned by
dbSNPrs863223917
ebirs863223917
HLIrs863223917
Exacrs863223917
Varsomers863223917
Maprs863223917
PheGenIrs863223917
hapmaprs863223917
1000 genomesrs863223917
hgdprs863223917
ensemblrs863223917
gopubmedrs863223917
geneviewrs863223917
scholarrs863223917
googlers863223917
pharmgkbrs863223917
gwascentralrs863223917
openSNPrs863223917
23andMers863223917
23andMe allrs863223917
SNP Nexus

SNPshotrs863223917
SNPdbers863223917
MSV3drs863223917
GWAS Ctlgrs863223917
Max Magnitude0
ClinVar
Risk rs863223917(G;G)
Alt rs863223917(G;G)
Reference rs863223917(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MRPL43 C10orf2
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.102748305G>C
CLNSRC
CLNACC RCV000195756.1,