rs121918669
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs121918669(G;T) |
Make rs121918669(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 115033456 |
Gene | TSHB |
is a | snp |
is | mentioned by |
dbSNP | rs121918669 |
dbSNP (classic) | rs121918669 |
ClinGen | rs121918669 |
ebi | rs121918669 |
HLI | rs121918669 |
Exac | rs121918669 |
Gnomad | rs121918669 |
Varsome | rs121918669 |
LitVar | rs121918669 |
Map | rs121918669 |
PheGenI | rs121918669 |
Biobank | rs121918669 |
1000 genomes | rs121918669 |
hgdp | rs121918669 |
ensembl | rs121918669 |
geneview | rs121918669 |
scholar | rs121918669 |
rs121918669 | |
pharmgkb | rs121918669 |
gwascentral | rs121918669 |
openSNP | rs121918669 |
23andMe | rs121918669 |
SNPshot | rs121918669 |
SNPdbe | rs121918669 |
MSV3d | rs121918669 |
GWAS Ctlg | rs121918669 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121918669(A;A) rs121918669(T;T) |
Alt | rs121918669(A;A) rs121918669(T;T) |
Reference | Rs121918669(G;G) |
Significance | Pathogenic |
Disease | Secondary hypothyroidism |
Variation | info |
Gene | TSHB |
CLNDBN | Secondary hypothyroidism |
Reversed | 0 |
HGVS | NC_000001.10:g.115576077G>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000013522.22, |