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rs869312930

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312930(A;A)
Make rs869312930(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position173833432
GeneDARS2
is asnp
is mentioned by
dbSNPrs869312930
ebirs869312930
HLIrs869312930
Exacrs869312930
Varsomers869312930
Maprs869312930
PheGenIrs869312930
hapmaprs869312930
1000 genomesrs869312930
hgdprs869312930
ensemblrs869312930
gopubmedrs869312930
geneviewrs869312930
scholarrs869312930
googlers869312930
pharmgkbrs869312930
gwascentralrs869312930
openSNPrs869312930
23andMers869312930
23andMe allrs869312930
SNP Nexus

SNPshotrs869312930
SNPdbers869312930
MSV3drs869312930
GWAS Ctlgrs869312930
Max Magnitude0
ClinVar
Risk rs869312930(A;A)
Alt rs869312930(A;A)
Reference rs869312930(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene DARS2
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.173802570G>A
CLNSRC
CLNACC RCV000210580.1,