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rs780936696

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs780936696(A;T)
Make rs780936696(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position3481601
GeneASPA, SPATA22
is asnp
is mentioned by
dbSNPrs780936696
ebirs780936696
HLIrs780936696
Exacrs780936696
Varsomers780936696
Maprs780936696
PheGenIrs780936696
hapmaprs780936696
1000 genomesrs780936696
hgdprs780936696
ensemblrs780936696
gopubmedrs780936696
geneviewrs780936696
scholarrs780936696
googlers780936696
pharmgkbrs780936696
gwascentralrs780936696
openSNPrs780936696
23andMers780936696
23andMe allrs780936696
SNP Nexus

SNPshotrs780936696
SNPdbers780936696
MSV3drs780936696
GWAS Ctlgrs780936696
Max Magnitude0
ClinVar
Risk rs780936696(T;T)
Alt rs780936696(T;T)
Reference rs780936696(A;A)
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.3384895A>T
CLNSRC
CLNACC RCV000169526.1,