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rs1057517905

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517905(A;A)
Make rs1057517905(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154092190
GeneMECP2
is asnp
is mentioned by
dbSNPrs1057517905
dbSNP (old)rs1057517905
ClinGenrs1057517905
ebirs1057517905
HLIrs1057517905
Exacrs1057517905
Gnomadrs1057517905
Varsomers1057517905
Maprs1057517905
PheGenIrs1057517905
Biobankrs1057517905
1000 genomesrs1057517905
hgdprs1057517905
ensemblrs1057517905
gopubmedrs1057517905
geneviewrs1057517905
scholarrs1057517905
googlers1057517905
pharmgkbrs1057517905
gwascentralrs1057517905
openSNPrs1057517905
23andMers1057517905
23andMe allrs1057517905
SNPshotrs1057517905
SNPdbers1057517905
MSV3drs1057517905
GWAS Ctlgrs1057517905
Max Magnitude0
ClinVar
Risk rs1057517905(A;A)
Alt rs1057517905(A;A)
Reference Rs1057517905(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153357648C>T
CLNSRC
CLNACC RCV000413833.1,