rs606231183

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs606231183(C;C)

Make rs606231183(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

129841774

Gene

ZDHHC9

is a	snp
is	mentioned by
dbSNP	rs606231183
dbSNP (classic)	rs606231183
ClinGen	rs606231183
ebi	rs606231183
HLI	rs606231183
Exac	rs606231183
Gnomad	rs606231183
Varsome	rs606231183
LitVar	rs606231183
Map	rs606231183
PheGenI	rs606231183
Biobank	rs606231183
1000 genomes	rs606231183
hgdp	rs606231183
ensembl	rs606231183
geneview	rs606231183
scholar	rs606231183
google	rs606231183
pharmgkb	rs606231183
gwascentral	rs606231183
openSNP	rs606231183
23andMe	rs606231183
SNPshot	rs606231183
SNPdbe	rs606231183
MSV3d	rs606231183
GWAS Ctlg	rs606231183

Max Magnitude

0

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,