rs876657396
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs876657396(C;G) |
Make rs876657396(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 40089416 |
Gene | THRA |
is a | snp |
is | mentioned by |
dbSNP | rs876657396 |
dbSNP (classic) | rs876657396 |
ClinGen | rs876657396 |
ebi | rs876657396 |
HLI | rs876657396 |
Exac | rs876657396 |
Gnomad | rs876657396 |
Varsome | rs876657396 |
LitVar | rs876657396 |
Map | rs876657396 |
PheGenI | rs876657396 |
Biobank | rs876657396 |
1000 genomes | rs876657396 |
hgdp | rs876657396 |
ensembl | rs876657396 |
geneview | rs876657396 |
scholar | rs876657396 |
rs876657396 | |
pharmgkb | rs876657396 |
gwascentral | rs876657396 |
openSNP | rs876657396 |
23andMe | rs876657396 |
SNPshot | rs876657396 |
SNPdbe | rs876657396 |
MSV3d | rs876657396 |
GWAS Ctlg | rs876657396 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876657396(G;G) |
Alt | rs876657396(G;G) |
Reference | Rs876657396(C;C) |
Significance | Pathogenic |
Disease | Hypothyroidism |
Variation | info |
Gene | THRA |
CLNDBN | Hypothyroidism, congenital, nongoitrous, 6 |
Reversed | 0 |
HGVS | NC_000017.10:g.38245669C>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000172855.3, |