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rs2075596

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2075596(A;G)
Make rs2075596(G;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position154031941
GeneMECP2
is asnp
is mentioned by
dbSNPrs2075596
ebirs2075596
HLIrs2075596
Exacrs2075596
Varsomers2075596
Maprs2075596
PheGenIrs2075596
hapmaprs2075596
1000 genomesrs2075596
hgdprs2075596
ensemblrs2075596
gopubmedrs2075596
geneviewrs2075596
scholarrs2075596
googlers2075596
pharmgkbrs2075596
gwascentralrs2075596
openSNPrs2075596
23andMers2075596
23andMe allrs2075596
SNP Nexus

SNPshotrs2075596
SNPdbers2075596
MSV3drs2075596
GWAS Ctlgrs2075596
Max Magnitude0
? (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,