rs1060499620

Orientation

minus

Stabilized

minus

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

Make rs1060499620(-;AG)

Make rs1060499620(AG;AG)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

154030803

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs1060499620
dbSNP (classic)	rs1060499620
ClinGen	rs1060499620
ebi	rs1060499620
HLI	rs1060499620
Exac	rs1060499620
Gnomad	rs1060499620
Varsome	rs1060499620
LitVar	rs1060499620
Map	rs1060499620
PheGenI	rs1060499620
Biobank	rs1060499620
1000 genomes	rs1060499620
hgdp	rs1060499620
ensembl	rs1060499620
geneview	rs1060499620
scholar	rs1060499620
google	rs1060499620
pharmgkb	rs1060499620
gwascentral	rs1060499620
openSNP	rs1060499620
23andMe	rs1060499620
SNPshot	rs1060499620
SNPdbe	rs1060499620
MSV3d	rs1060499620
GWAS Ctlg	rs1060499620

Max Magnitude

0

ClinVar
Risk	rs1060499620(AG;AG)
Alt	rs1060499620(AG;AG)
Reference	Rs1060499620(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	MECP2
CLNDBN	Rett syndrome
Reversed	1
HGVS	NC_000023.10:g.153296254_153296255insCT
CLNSRC
CLNACC	RCV000445567.1,