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rs869312918

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312918(A;A)
Make rs869312918(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position173825357
GeneCENPL, DARS2
is asnp
is mentioned by
dbSNPrs869312918
ebirs869312918
HLIrs869312918
Exacrs869312918
Varsomers869312918
Maprs869312918
PheGenIrs869312918
hapmaprs869312918
1000 genomesrs869312918
hgdprs869312918
ensemblrs869312918
gopubmedrs869312918
geneviewrs869312918
scholarrs869312918
googlers869312918
pharmgkbrs869312918
gwascentralrs869312918
openSNPrs869312918
23andMers869312918
23andMe allrs869312918
SNP Nexus

SNPshotrs869312918
SNPdbers869312918
MSV3drs869312918
GWAS Ctlgrs869312918
Max Magnitude0
ClinVar
Risk rs869312918(A;A)
Alt rs869312918(A;A)
Reference rs869312918(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene DARS2 CENPL
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.173794495G>A
CLNSRC
CLNACC RCV000210734.1,