rs28933691

Orientation

plus

Stabilized

plus

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

Make rs28933691(A;A)

Make rs28933691(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

47915182

Gene

ZNF81

is a	snp
is	mentioned by
dbSNP	rs28933691
dbSNP (classic)	rs28933691
ClinGen	rs28933691
ebi	rs28933691
HLI	rs28933691
Exac	rs28933691
Gnomad	rs28933691
Varsome	rs28933691
LitVar	rs28933691
Map	rs28933691
PheGenI	rs28933691
Biobank	rs28933691
1000 genomes	rs28933691
hgdp	rs28933691
ensembl	rs28933691
geneview	rs28933691
scholar	rs28933691
google	rs28933691
pharmgkb	rs28933691
gwascentral	rs28933691
openSNP	rs28933691
23andMe	rs28933691
SNPshot	rs28933691
SNPdbe	rs28933691
MSV3d	rs28933691
GWAS Ctlg	rs28933691

Max Magnitude

0

OMIM	314998
Desc	MENTAL RETARDATION, X-LINKED 45
Variant	0001
Related	also

ClinVar
Risk	rs28933691(A;A)
Alt	rs28933691(A;A)
Reference	Rs28933691(G;G)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	ZNF81
CLNDBN	Mental retardation, X-linked 45
Reversed	0
HGVS	NC_000023.10:g.47774581G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000010413.3,