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rs587777769

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777769(-;-)
Make rs587777769(-;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position109625368
GeneAMPD2
is asnp
is mentioned by
dbSNPrs587777769
ebirs587777769
HLIrs587777769
Exacrs587777769
Varsomers587777769
Maprs587777769
PheGenIrs587777769
hapmaprs587777769
1000 genomesrs587777769
hgdprs587777769
ensemblrs587777769
gopubmedrs587777769
geneviewrs587777769
scholarrs587777769
googlers587777769
pharmgkbrs587777769
gwascentralrs587777769
openSNPrs587777769
23andMers587777769
23andMe allrs587777769
SNP Nexus

SNPshotrs587777769
SNPdbers587777769
MSV3drs587777769
GWAS Ctlgrs587777769
Max Magnitude0
ClinVar
Risk rs587777769(;)
Alt rs587777769(;)
Reference rs587777769(T;T)
Significance Pathogenic
Disease Spastic paraplegia 63
Variation info
Gene AMPD2
CLNDBN Spastic paraplegia 63, autosomal recessive
Reversed 0
HGVS NC_000001.10:g.110167990delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000087328.8,