rs1057519216

Orientation

minus

Stabilized

minus

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

Make rs1057519216(G;T)

Make rs1057519216(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

154030582

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs1057519216
dbSNP (classic)	rs1057519216
ClinGen	rs1057519216
ebi	rs1057519216
HLI	rs1057519216
Exac	rs1057519216
Gnomad	rs1057519216
Varsome	rs1057519216
LitVar	rs1057519216
Map	rs1057519216
PheGenI	rs1057519216
Biobank	rs1057519216
1000 genomes	rs1057519216
hgdp	rs1057519216
ensembl	rs1057519216
geneview	rs1057519216
scholar	rs1057519216
google	rs1057519216
pharmgkb	rs1057519216
gwascentral	rs1057519216
openSNP	rs1057519216
23andMe	rs1057519216
SNPshot	rs1057519216
SNPdbe	rs1057519216
MSV3d	rs1057519216
GWAS Ctlg	rs1057519216

Max Magnitude

0

ClinVar
Risk	rs1057519216(T;T)
Alt	rs1057519216(T;T)
Reference	Rs1057519216(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MECP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.153296033C>A
CLNSRC
CLNACC	RCV000415905.1,