rs61751443

Orientation

minus

Stabilized

minus

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

Make rs61751443(G;T)

Make rs61751443(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

154030911

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs61751443
dbSNP (classic)	rs61751443
ClinGen	rs61751443
ebi	rs61751443
HLI	rs61751443
Exac	rs61751443
Gnomad	rs61751443
Varsome	rs61751443
LitVar	rs61751443
Map	rs61751443
PheGenI	rs61751443
Biobank	rs61751443
1000 genomes	rs61751443
hgdp	rs61751443
ensembl	rs61751443
geneview	rs61751443
scholar	rs61751443
google	rs61751443
pharmgkb	rs61751443
gwascentral	rs61751443
openSNP	rs61751443
23andMe	rs61751443
SNPshot	rs61751443
SNPdbe	rs61751443
MSV3d	rs61751443
GWAS Ctlg	rs61751443

Max Magnitude

0

ClinVar
Risk	rs61751443(A;A) rs61751443(T;T)
Alt	rs61751443(A;A) rs61751443(T;T)
Reference	Rs61751443(G;G)
Significance	Other
Disease	not provided Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	not provided Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296362C>A; NC_000023.10:g.153296362C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000133291.1, RCV000133290.3, RCV000256087.1,