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rs122461161

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs122461161(A;A)
Make rs122461161(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position29955189
GeneIL1RAPL1
is asnp
is mentioned by
dbSNPrs122461161
ebirs122461161
HLIrs122461161
Exacrs122461161
Varsomers122461161
Maprs122461161
PheGenIrs122461161
hapmaprs122461161
1000 genomesrs122461161
hgdprs122461161
ensemblrs122461161
gopubmedrs122461161
geneviewrs122461161
scholarrs122461161
googlers122461161
pharmgkbrs122461161
gwascentralrs122461161
openSNPrs122461161
23andMers122461161
23andMe allrs122461161
SNP Nexus

SNPshotrs122461161
SNPdbers122461161
MSV3drs122461161
GWAS Ctlgrs122461161
Max Magnitude0
OMIM300206
Desc
Variant0002
Relatedalso
ClinVar
Risk rs122461161(A;A)
Alt rs122461161(A;A)
Reference rs122461161(G;G)
Significance Pathogenic
Disease Mental retardation 21
Variation info
Gene IL1RAPL1
CLNDBN Mental retardation 21, X-linked
Reversed 0
HGVS NC_000023.10:g.29973306G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012236.24,