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rs672601375

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs672601375(A;G)
Make rs672601375(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position168486499
GeneRARS
is asnp
is mentioned by
dbSNPrs672601375
ebirs672601375
HLIrs672601375
Exacrs672601375
Varsomers672601375
Maprs672601375
PheGenIrs672601375
hapmaprs672601375
1000 genomesrs672601375
hgdprs672601375
ensemblrs672601375
gopubmedrs672601375
geneviewrs672601375
scholarrs672601375
googlers672601375
pharmgkbrs672601375
gwascentralrs672601375
openSNPrs672601375
23andMers672601375
23andMe allrs672601375
SNP Nexus

SNPshotrs672601375
SNPdbers672601375
MSV3drs672601375
GWAS Ctlgrs672601375
Max Magnitude0
ClinVar
Risk rs672601375(G;G)
Alt rs672601375(G;G)
Reference rs672601375(A;A)
Significance Pathogenic
Disease Leukodystrophy
Variation info
Gene RARS
CLNDBN Leukodystrophy, hypomyelinating, 9
Reversed 0
HGVS NC_000005.9:g.167913504A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000149501.3,