rs879255362
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs879255362(G;T) |
Make rs879255362(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 64917850 |
Gene | ZC4H2 |
is a | snp |
is | mentioned by |
dbSNP | rs879255362 |
dbSNP (classic) | rs879255362 |
ClinGen | rs879255362 |
ebi | rs879255362 |
HLI | rs879255362 |
Exac | rs879255362 |
Gnomad | rs879255362 |
Varsome | rs879255362 |
LitVar | rs879255362 |
Map | rs879255362 |
PheGenI | rs879255362 |
Biobank | rs879255362 |
1000 genomes | rs879255362 |
hgdp | rs879255362 |
ensembl | rs879255362 |
geneview | rs879255362 |
scholar | rs879255362 |
rs879255362 | |
pharmgkb | rs879255362 |
gwascentral | rs879255362 |
openSNP | rs879255362 |
23andMe | rs879255362 |
SNPshot | rs879255362 |
SNPdbe | rs879255362 |
MSV3d | rs879255362 |
GWAS Ctlg | rs879255362 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879255362(T;T) |
Alt | rs879255362(T;T) |
Reference | Rs879255362(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ZC4H2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000023.10:g.64137730C>A |
CLNSRC | |
CLNACC | RCV000238874.1, |