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rs786205133

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205133(A;G)
Make rs786205133(G;G)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position74592248
GeneRLIM
is asnp
is mentioned by
dbSNPrs786205133
ClinGenrs786205133
ebirs786205133
HLIrs786205133
Exacrs786205133
Varsomers786205133
Maprs786205133
PheGenIrs786205133
hapmaprs786205133
1000 genomesrs786205133
hgdprs786205133
ensemblrs786205133
gopubmedrs786205133
geneviewrs786205133
scholarrs786205133
googlers786205133
pharmgkbrs786205133
gwascentralrs786205133
openSNPrs786205133
23andMers786205133
23andMe allrs786205133
SNP Nexus

SNPshotrs786205133
SNPdbers786205133
MSV3drs786205133
GWAS Ctlgrs786205133
Max Magnitude0
ClinVar
Risk rs786205133(G;G)
Alt rs786205133(G;G)
Reference Rs786205133(A;A)
Significance Pathogenic
Disease Non-syndromic X-linked intellectual disability Mental retardation
Variation info
Gene RLIM
CLNDBN Non-syndromic X-linked intellectual disability Mental retardation, X-linked 61
Reversed 1
HGVS NC_000023.10:g.73812083T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000170337.1, RCV000207499.2,