rs63749030
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCA;CCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCA) | 0 | common in clinvar |
Make rs63749030(-;-) |
Make rs63749030(-;CCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCA) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | X |
Position | 154030627 |
Gene | MECP2 |
is a | snp |
is | mentioned by |
dbSNP | rs63749030 |
dbSNP (classic) | rs63749030 |
ClinGen | rs63749030 |
ebi | rs63749030 |
HLI | rs63749030 |
Exac | rs63749030 |
Gnomad | rs63749030 |
Varsome | rs63749030 |
LitVar | rs63749030 |
Map | rs63749030 |
PheGenI | rs63749030 |
Biobank | rs63749030 |
1000 genomes | rs63749030 |
hgdp | rs63749030 |
ensembl | rs63749030 |
geneview | rs63749030 |
scholar | rs63749030 |
rs63749030 | |
pharmgkb | rs63749030 |
gwascentral | rs63749030 |
openSNP | rs63749030 |
23andMe | rs63749030 |
SNPshot | rs63749030 |
SNPdbe | rs63749030 |
MSV3d | rs63749030 |
GWAS Ctlg | rs63749030 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs63749030(-;-) |
Alt | rs63749030(-;-) |
Reference | Rs63749030(CCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCA;CCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCA) |
Significance | Pathogenic |
Disease | Rett syndrome |
Variation | info |
Gene | MECP2 |
CLNDBN | Rett syndrome |
Reversed | 1 |
HGVS | NC_000023.10:g.153296078_153296120del43 |
CLNSRC | |
CLNACC | RCV000132907.2, |