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rs587777858

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777858(-;-)
Make rs587777858(-;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position95610272
GeneALDH18A1
is asnp
is mentioned by
dbSNPrs587777858
ebirs587777858
HLIrs587777858
Exacrs587777858
Varsomers587777858
Maprs587777858
PheGenIrs587777858
hapmaprs587777858
1000 genomesrs587777858
hgdprs587777858
ensemblrs587777858
gopubmedrs587777858
geneviewrs587777858
scholarrs587777858
googlers587777858
pharmgkbrs587777858
gwascentralrs587777858
openSNPrs587777858
23andMers587777858
23andMe allrs587777858
SNP Nexus

SNPshotrs587777858
SNPdbers587777858
MSV3drs587777858
GWAS Ctlgrs587777858
Max Magnitude0
ClinVar
Risk rs587777858(;)
Alt rs587777858(;)
Reference rs587777858(G;G)
Significance Pathogenic
Disease Cutis laxa-corneal clouding-oligophrenia syndrome
Variation info
Gene ALDH18A1
CLNDBN Cutis laxa-corneal clouding-oligophrenia syndrome
Reversed 0
HGVS NC_000010.10:g.97370029delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000144700.3,