rs2075596

Orientation

plus

Stabilized

plus

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

Make rs2075596(A;G)

Make rs2075596(G;G)

Reference

GRCh38 38.1/142

Chromosome

X

Position

154031941

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs2075596
dbSNP (classic)	rs2075596
ClinGen	rs2075596
ebi	rs2075596
HLI	rs2075596
Exac	rs2075596
Gnomad	rs2075596
Varsome	rs2075596
LitVar	rs2075596
Map	rs2075596
PheGenI	rs2075596
Biobank	rs2075596
1000 genomes	rs2075596
hgdp	rs2075596
ensembl	rs2075596
geneview	rs2075596
scholar	rs2075596
google	rs2075596
pharmgkb	rs2075596
gwascentral	rs2075596
openSNP	rs2075596
23andMe	rs2075596
SNPshot	rs2075596
SNPdbe	rs2075596
MSV3d	rs2075596
GWAS Ctlg	rs2075596

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 25458699] Variants in IRAK1-MECP2 region confer susceptibility to autoimmune thyroid diseases

ClinVar
Risk	rs2075596(G;G)
Alt	rs2075596(G;G)
Reference	Rs2075596(A;A)
Significance	Non-pathogenic
Disease	not provided not specified
Variation	info
Gene	MECP2
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000023.10:g.153297392A>G
CLNSRC	ClinVar
CLNACC	RCV000144103.1, RCV000170089.1,