Have questions? Visit https://www.reddit.com/r/SNPedia

rs797045695

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045695(-;TCAAGAT)
Make rs797045695(TCAAGAT;TCAAGAT)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154031156
GeneMECP2
is asnp
is mentioned by
dbSNPrs797045695
ClinGenrs797045695
ebirs797045695
HLIrs797045695
Exacrs797045695
Varsomers797045695
Maprs797045695
PheGenIrs797045695
hapmaprs797045695
1000 genomesrs797045695
hgdprs797045695
ensemblrs797045695
gopubmedrs797045695
geneviewrs797045695
scholarrs797045695
googlers797045695
pharmgkbrs797045695
gwascentralrs797045695
openSNPrs797045695
23andMers797045695
23andMe allrs797045695
SNP Nexus

SNPshotrs797045695
SNPdbers797045695
MSV3drs797045695
GWAS Ctlgrs797045695
Max Magnitude0
ClinVar
Risk rs797045695(TCAAGAT;TCAAGAT)
Alt rs797045695(TCAAGAT;TCAAGAT)
Reference Rs797045695(-;-)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296608_153296614dupATCTTGA
CLNSRC
CLNACC RCV000195260.1,