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rs587777225

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CATG;CATG) 0 common in clinvar
Make rs587777225(-;-)
Make rs587777225(-;CATG)
ReferenceGRCh38 38.1/142
Chromosome15
Position100573885
GeneLINS
is asnp
is mentioned by
dbSNPrs587777225
ebirs587777225
HLIrs587777225
Exacrs587777225
Varsomers587777225
Maprs587777225
PheGenIrs587777225
hapmaprs587777225
1000 genomesrs587777225
hgdprs587777225
ensemblrs587777225
gopubmedrs587777225
geneviewrs587777225
scholarrs587777225
googlers587777225
pharmgkbrs587777225
gwascentralrs587777225
openSNPrs587777225
23andMers587777225
23andMe allrs587777225
SNP Nexus

SNPshotrs587777225
SNPdbers587777225
MSV3drs587777225
GWAS Ctlgrs587777225
Max Magnitude0
ClinVar
Risk rs587777225(;)
Alt rs587777225(;)
Reference rs587777225(CATG;CATG)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene LINS
CLNDBN Mental retardation, autosomal recessive 27
Reversed 1
HGVS NC_000015.9:g.101114090_101114093delCATG
CLNSRC OMIM Allelic Variant
CLNACC RCV000106305.2,