rs1057522038

Orientation

minus

Stabilized

minus

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

Make rs1057522038(A;G)

Make rs1057522038(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

154030921

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs1057522038
dbSNP (classic)	rs1057522038
ClinGen	rs1057522038
ebi	rs1057522038
HLI	rs1057522038
Exac	rs1057522038
Gnomad	rs1057522038
Varsome	rs1057522038
LitVar	rs1057522038
Map	rs1057522038
PheGenI	rs1057522038
Biobank	rs1057522038
1000 genomes	rs1057522038
hgdp	rs1057522038
ensembl	rs1057522038
geneview	rs1057522038
scholar	rs1057522038
google	rs1057522038
pharmgkb	rs1057522038
gwascentral	rs1057522038
openSNP	rs1057522038
23andMe	rs1057522038
SNPshot	rs1057522038
SNPdbe	rs1057522038
MSV3d	rs1057522038
GWAS Ctlg	rs1057522038

Max Magnitude

0

ClinVar
Risk	rs1057522038(G;G)
Alt	rs1057522038(G;G)
Reference	Rs1057522038(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MECP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.153296372T>C
CLNSRC
CLNACC	RCV000438431.1,