Have questions? Visit https://www.reddit.com/r/SNPedia

rs199422235

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199422235(C;C)
Make rs199422235(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position53211867
GeneKDM5C
is asnp
is mentioned by
dbSNPrs199422235
ebirs199422235
HLIrs199422235
Exacrs199422235
Varsomers199422235
Maprs199422235
PheGenIrs199422235
hapmaprs199422235
1000 genomesrs199422235
hgdprs199422235
ensemblrs199422235
gopubmedrs199422235
geneviewrs199422235
scholarrs199422235
googlers199422235
pharmgkbrs199422235
gwascentralrs199422235
openSNPrs199422235
23andMers199422235
23andMe allrs199422235
SNP Nexus

SNPshotrs199422235
SNPdbers199422235
MSV3drs199422235
GWAS Ctlgrs199422235
Max Magnitude0
ClinVar
Risk rs199422235(C;C)
Alt rs199422235(C;C)
Reference rs199422235(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene KDM5C
CLNDBN Mental retardation, syndromic, Claes-Jensen type, X-linked
Reversed 1
HGVS NC_000023.10:g.53241049C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010428.4,