rs1057517905

Orientation

minus

Stabilized

minus

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

Make rs1057517905(A;A)

Make rs1057517905(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

154092190

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs1057517905
dbSNP (classic)	rs1057517905
ClinGen	rs1057517905
ebi	rs1057517905
HLI	rs1057517905
Exac	rs1057517905
Gnomad	rs1057517905
Varsome	rs1057517905
LitVar	rs1057517905
Map	rs1057517905
PheGenI	rs1057517905
Biobank	rs1057517905
1000 genomes	rs1057517905
hgdp	rs1057517905
ensembl	rs1057517905
geneview	rs1057517905
scholar	rs1057517905
google	rs1057517905
pharmgkb	rs1057517905
gwascentral	rs1057517905
openSNP	rs1057517905
23andMe	rs1057517905
SNPshot	rs1057517905
SNPdbe	rs1057517905
MSV3d	rs1057517905
GWAS Ctlg	rs1057517905

Max Magnitude

0

ClinVar
Risk	rs1057517905(A;A)
Alt	rs1057517905(A;A)
Reference	Rs1057517905(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MECP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.153357648C>T
CLNSRC
CLNACC	RCV000413833.1,