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rs606231183

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231183(C;C)
Make rs606231183(C;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position129841774
GeneZDHHC9
is asnp
is mentioned by
dbSNPrs606231183
ebirs606231183
HLIrs606231183
Exacrs606231183
Varsomers606231183
Maprs606231183
PheGenIrs606231183
hapmaprs606231183
1000 genomesrs606231183
hgdprs606231183
ensemblrs606231183
gopubmedrs606231183
geneviewrs606231183
scholarrs606231183
googlers606231183
pharmgkbrs606231183
gwascentralrs606231183
openSNPrs606231183
23andMers606231183
23andMe allrs606231183
SNP Nexus

SNPshotrs606231183
SNPdbers606231183
MSV3drs606231183
GWAS Ctlgrs606231183
Max Magnitude0
ClinVar
Risk rs606231183(C;C)
Alt rs606231183(C;C)
Reference rs606231183(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ZDHHC9
CLNDBN Mental retardation, X-linked, syndromic, raymond type
Reversed 1
HGVS NC_000023.10:g.128975750C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000011456.9,