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rs28935168

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0
Make rs28935168(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154032286
GeneMECP2
is asnp
is mentioned by
dbSNPrs28935168
ebirs28935168
HLIrs28935168
Exacrs28935168
Varsomers28935168
Maprs28935168
PheGenIrs28935168
hapmaprs28935168
1000 genomesrs28935168
hgdprs28935168
ensemblrs28935168
gopubmedrs28935168
geneviewrs28935168
scholarrs28935168
googlers28935168
pharmgkbrs28935168
gwascentralrs28935168
openSNPrs28935168
23andMers28935168
23andMe allrs28935168
SNP Nexus

SNPshotrs28935168
SNPdbers28935168
MSV3drs28935168
GWAS Ctlgrs28935168
Max Magnitude0
OMIM300005
DescRETT SYNDROME
Variant0027
Relatedalso
Neighborrs28934907
Distance18


ClinVar
Risk rs28935168(G;G)
Alt rs28935168(G;G)
Reference rs28935168(C;C)
Significance Other
Disease Rett syndrome not specified
Variation info
Gene MECP2
CLNDBN Rett syndrome not specified
Reversed 1
HGVS NC_000023.10:g.153297737G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012608.23, RCV000168679.1,