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rs587777226

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAGGT;AAAGGT) 0 common in clinvar
(CCTTT;CCTTT) 0 common in clinvar
Make rs587777226(-;-)
Make rs587777226(-;CCTTT)
ReferenceGRCh38 38.1/142
Chromosome15
Position100573650
GeneLINS
is asnp
is mentioned by
dbSNPrs587777226
ebirs587777226
HLIrs587777226
Exacrs587777226
Varsomers587777226
Maprs587777226
PheGenIrs587777226
hapmaprs587777226
1000 genomesrs587777226
hgdprs587777226
ensemblrs587777226
gopubmedrs587777226
geneviewrs587777226
scholarrs587777226
googlers587777226
pharmgkbrs587777226
gwascentralrs587777226
openSNPrs587777226
23andMers587777226
23andMe allrs587777226
SNP Nexus

SNPshotrs587777226
SNPdbers587777226
MSV3drs587777226
GWAS Ctlgrs587777226
Max Magnitude0
ClinVar
Risk rs587777226(CCTTTT,T;CCTTTT,T)
Alt rs587777226(CCTTTT,T;CCTTTT,T)
Reference rs587777226(AAAGGT;AAAGGT)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene LINS
CLNDBN Mental retardation, autosomal recessive 27
Reversed 1
HGVS NC_000015.9:g.101113855_101113859delCCTTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000106306.2,