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rs61750235

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs61750235(-;-)
Make rs61750235(-;CAGGAAGC)
Make rs61750235(CAGGAAGC;CAGGAAGC)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031064
GeneMECP2
is asnp
is mentioned by
dbSNPrs61750235
ebirs61750235
HLIrs61750235
Exacrs61750235
Varsomers61750235
Maprs61750235
PheGenIrs61750235
hapmaprs61750235
1000 genomesrs61750235
hgdprs61750235
ensemblrs61750235
gopubmedrs61750235
geneviewrs61750235
scholarrs61750235
googlers61750235
pharmgkbrs61750235
gwascentralrs61750235
openSNPrs61750235
23andMers61750235
23andMe allrs61750235
SNP Nexus

SNPshotrs61750235
SNPdbers61750235
MSV3drs61750235
GWAS Ctlgrs61750235
Max Magnitude0
ClinVar
Risk rs61750235(CAGGAAGC;CAGGAAGC)
Alt rs61750235(CAGGAAGC;CAGGAAGC)
Reference rs61750235(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296516_153296523dupGCTTCCTG
CLNSRC
CLNACC RCV000133233.2,