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rs369398935

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369398935(A;A)
Make rs369398935(A;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position168516860
GeneRARS
is asnp
is mentioned by
dbSNPrs369398935
ebirs369398935
HLIrs369398935
Exacrs369398935
Varsomers369398935
Maprs369398935
PheGenIrs369398935
hapmaprs369398935
1000 genomesrs369398935
hgdprs369398935
ensemblrs369398935
gopubmedrs369398935
geneviewrs369398935
scholarrs369398935
googlers369398935
pharmgkbrs369398935
gwascentralrs369398935
openSNPrs369398935
23andMers369398935
23andMe allrs369398935
SNP Nexus

SNPshotrs369398935
SNPdbers369398935
MSV3drs369398935
GWAS Ctlgrs369398935
Max Magnitude0
ClinVar
Risk rs369398935(A;A)
Alt rs369398935(A;A)
Reference rs369398935(G;G)
Significance Pathogenic
Disease Leukodystrophy
Variation info
Gene RARS
CLNDBN Leukodystrophy, hypomyelinating, 9
Reversed 0
HGVS NC_000005.9:g.167943865G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000149502.3,