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rs786204620

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs786204620(-;-)
Make rs786204620(-;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position3481610
GeneASPA, SPATA22
is asnp
is mentioned by
dbSNPrs786204620
ebirs786204620
HLIrs786204620
Exacrs786204620
Varsomers786204620
Maprs786204620
PheGenIrs786204620
hapmaprs786204620
1000 genomesrs786204620
hgdprs786204620
ensemblrs786204620
gopubmedrs786204620
geneviewrs786204620
scholarrs786204620
googlers786204620
pharmgkbrs786204620
gwascentralrs786204620
openSNPrs786204620
23andMers786204620
23andMe allrs786204620
SNP Nexus

SNPshotrs786204620
SNPdbers786204620
MSV3drs786204620
GWAS Ctlgrs786204620
Max Magnitude0
ClinVar
Risk rs786204620(;)
Alt rs786204620(;)
Reference rs786204620(AT;AT)
Significance Probable-Pathogenic
Disease Spongy degeneration of central nervous system
Variation info
Gene ASPA SPATA22
CLNDBN Spongy degeneration of central nervous system
Reversed 0
HGVS NC_000017.10:g.3384904_3384905delAT
CLNSRC
CLNACC RCV000169388.1,