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rs766328537

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs766328537(A;A)
Make rs766328537(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position3476238
GeneASPA, SPATA22
is asnp
is mentioned by
dbSNPrs766328537
ebirs766328537
HLIrs766328537
Exacrs766328537
Varsomers766328537
Maprs766328537
PheGenIrs766328537
hapmaprs766328537
1000 genomesrs766328537
hgdprs766328537
ensemblrs766328537
gopubmedrs766328537
geneviewrs766328537
scholarrs766328537
googlers766328537
pharmgkbrs766328537
gwascentralrs766328537
openSNPrs766328537
23andMers766328537
23andMe allrs766328537
SNP Nexus

SNPshotrs766328537
SNPdbers766328537
MSV3drs766328537
GWAS Ctlgrs766328537
Max Magnitude0
ClinVar
Risk rs766328537(A;A)
Alt rs766328537(A;A)
Reference rs766328537(G;G)
Significance Probable-Pathogenic
Disease Spongy degeneration of central nervous system
Variation info
Gene SPATA22 ASPA
CLNDBN Spongy degeneration of central nervous system
Reversed 0
HGVS NC_000017.10:g.3379532G>A
CLNSRC
CLNACC RCV000169243.1,