rs767354861
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs767354861(C;T) |
Make rs767354861(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 71375242 |
Gene | TAF1 |
is a | snp |
is | mentioned by |
dbSNP | rs767354861 |
dbSNP (classic) | rs767354861 |
ClinGen | rs767354861 |
ebi | rs767354861 |
HLI | rs767354861 |
Exac | rs767354861 |
Gnomad | rs767354861 |
Varsome | rs767354861 |
LitVar | rs767354861 |
Map | rs767354861 |
PheGenI | rs767354861 |
Biobank | rs767354861 |
1000 genomes | rs767354861 |
hgdp | rs767354861 |
ensembl | rs767354861 |
geneview | rs767354861 |
scholar | rs767354861 |
rs767354861 | |
pharmgkb | rs767354861 |
gwascentral | rs767354861 |
openSNP | rs767354861 |
23andMe | rs767354861 |
SNPshot | rs767354861 |
SNPdbe | rs767354861 |
MSV3d | rs767354861 |
GWAS Ctlg | rs767354861 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs767354861(T;T) |
Alt | rs767354861(T;T) |
Reference | Rs767354861(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TAF1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.70595092C>T |
CLNSRC | |
CLNACC | RCV000427808.1, |