rs267608598
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CC;CC) | 0 | common in clinvar |
Make rs267608598(-;-) |
Make rs267608598(-;CC) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | X |
Position | 154030665 |
Gene | MECP2 |
is a | snp |
is | mentioned by |
dbSNP | rs267608598 |
dbSNP (classic) | rs267608598 |
ClinGen | rs267608598 |
ebi | rs267608598 |
HLI | rs267608598 |
Exac | rs267608598 |
Gnomad | rs267608598 |
Varsome | rs267608598 |
LitVar | rs267608598 |
Map | rs267608598 |
PheGenI | rs267608598 |
Biobank | rs267608598 |
1000 genomes | rs267608598 |
hgdp | rs267608598 |
ensembl | rs267608598 |
geneview | rs267608598 |
scholar | rs267608598 |
rs267608598 | |
pharmgkb | rs267608598 |
gwascentral | rs267608598 |
openSNP | rs267608598 |
23andMe | rs267608598 |
SNPshot | rs267608598 |
SNPdbe | rs267608598 |
MSV3d | rs267608598 |
GWAS Ctlg | rs267608598 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs267608598(-;-) |
Alt | rs267608598(-;-) |
Reference | Rs267608598(CC;CC) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MECP2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000023.10:g.153296116_153296117delGG |
CLNSRC | |
CLNACC | RCV000132920.2, |