rs122463167
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs122463167(A;A) |
Make rs122463167(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 137567448 |
Gene | ZIC3 |
is a | snp |
is | mentioned by |
dbSNP | rs122463167 |
dbSNP (classic) | rs122463167 |
ClinGen | rs122463167 |
ebi | rs122463167 |
HLI | rs122463167 |
Exac | rs122463167 |
Gnomad | rs122463167 |
Varsome | rs122463167 |
LitVar | rs122463167 |
Map | rs122463167 |
PheGenI | rs122463167 |
Biobank | rs122463167 |
1000 genomes | rs122463167 |
hgdp | rs122463167 |
ensembl | rs122463167 |
geneview | rs122463167 |
scholar | rs122463167 |
rs122463167 | |
pharmgkb | rs122463167 |
gwascentral | rs122463167 |
openSNP | rs122463167 |
23andMe | rs122463167 |
SNPshot | rs122463167 |
SNPdbe | rs122463167 |
MSV3d | rs122463167 |
GWAS Ctlg | rs122463167 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs122463167(A;A) |
Alt | rs122463167(A;A) |
Reference | Rs122463167(T;T) |
Significance | Untested |
Disease | Heterotaxy |
Variation | info |
Gene | ZIC3 |
CLNDBN | Heterotaxy, visceral, X-linked |
Reversed | 0 |
HGVS | NC_000023.10:g.136649607T>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | SCV000032424.1, SCV000032424.1, |