rs797045018

Orientation

minus

Stabilized

minus

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

Make rs797045018(C;C)

Make rs797045018(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

123665715

Gene

THOC2

is a	snp
is	mentioned by
dbSNP	rs797045018
dbSNP (classic)	rs797045018
ClinGen	rs797045018
ebi	rs797045018
HLI	rs797045018
Exac	rs797045018
Gnomad	rs797045018
Varsome	rs797045018
LitVar	rs797045018
Map	rs797045018
PheGenI	rs797045018
Biobank	rs797045018
1000 genomes	rs797045018
hgdp	rs797045018
ensembl	rs797045018
geneview	rs797045018
scholar	rs797045018
google	rs797045018
pharmgkb	rs797045018
gwascentral	rs797045018
openSNP	rs797045018
23andMe	rs797045018
SNPshot	rs797045018
SNPdbe	rs797045018
MSV3d	rs797045018
GWAS Ctlg	rs797045018

Max Magnitude

0

ClinVar
Risk	rs797045018(C;C)
Alt	rs797045018(C;C)
Reference	Rs797045018(T;T)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	THOC2
CLNDBN	Mental retardation, X-linked 12
Reversed	1
HGVS	NC_000023.10:g.122799566A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000190530.2,