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rs672601372

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs672601372(A;G)
Make rs672601372(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position168486503
GeneRARS
is asnp
is mentioned by
dbSNPrs672601372
ebirs672601372
HLIrs672601372
Exacrs672601372
Varsomers672601372
Maprs672601372
PheGenIrs672601372
hapmaprs672601372
1000 genomesrs672601372
hgdprs672601372
ensemblrs672601372
gopubmedrs672601372
geneviewrs672601372
scholarrs672601372
googlers672601372
pharmgkbrs672601372
gwascentralrs672601372
openSNPrs672601372
23andMers672601372
23andMe allrs672601372
SNP Nexus

SNPshotrs672601372
SNPdbers672601372
MSV3drs672601372
GWAS Ctlgrs672601372
Max Magnitude0
ClinVar
Risk rs672601372(G;G)
Alt rs672601372(G;G)
Reference rs672601372(A;A)
Significance Pathogenic
Disease Leukodystrophy
Variation info
Gene RARS
CLNDBN Leukodystrophy, hypomyelinating, 9
Reversed 0
HGVS NC_000005.9:g.167913508A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000149498.3,