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rs797045693

From SNPedia

Orientationminus
Make rs797045693(-;-)
Make rs797045693(-;CG)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154097635
GeneMECP2
is asnp
is mentioned by
dbSNPrs797045693
ebirs797045693
HLIrs797045693
Exacrs797045693
Varsomers797045693
Maprs797045693
PheGenIrs797045693
hapmaprs797045693
1000 genomesrs797045693
hgdprs797045693
ensemblrs797045693
gopubmedrs797045693
geneviewrs797045693
scholarrs797045693
googlers797045693
pharmgkbrs797045693
gwascentralrs797045693
openSNPrs797045693
23andMers797045693
23andMe allrs797045693
SNP Nexus

SNPshotrs797045693
SNPdbers797045693
MSV3drs797045693
GWAS Ctlgrs797045693
Max Magnitude
ClinVar
Risk rs797045693(;)
Alt rs797045693(;)
Reference rs797045693(CG;CG)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153363092_153363093delCG
CLNSRC
CLNACC RCV000193898.1,