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rs754722529

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs754722529(A;A)
Make rs754722529(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position50626153
GeneARSA
is asnp
is mentioned by
dbSNPrs754722529
ebirs754722529
HLIrs754722529
Exacrs754722529
Varsomers754722529
Maprs754722529
PheGenIrs754722529
hapmaprs754722529
1000 genomesrs754722529
hgdprs754722529
ensemblrs754722529
gopubmedrs754722529
geneviewrs754722529
scholarrs754722529
googlers754722529
pharmgkbrs754722529
gwascentralrs754722529
openSNPrs754722529
23andMers754722529
23andMe allrs754722529
SNP Nexus

SNPshotrs754722529
SNPdbers754722529
MSV3drs754722529
GWAS Ctlgrs754722529
Max Magnitude0
ClinVar
Risk rs754722529(A,T;A,T)
Alt rs754722529(A,T;A,T)
Reference rs754722529(C;C)
Significance Probable-Pathogenic
Disease Metachromatic leukodystrophy
Variation info
Gene ARSA
CLNDBN Metachromatic leukodystrophy
Reversed 0
HGVS NC_000022.10:g.51064581C>T
CLNSRC
CLNACC RCV000169323.1,