rs121908871
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs121908871(G;G) |
Make rs121908871(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 81143228 |
Gene | LOC101928462, TSHR |
is a | snp |
is | mentioned by |
dbSNP | rs121908871 |
dbSNP (classic) | rs121908871 |
ClinGen | rs121908871 |
ebi | rs121908871 |
HLI | rs121908871 |
Exac | rs121908871 |
Gnomad | rs121908871 |
Varsome | rs121908871 |
LitVar | rs121908871 |
Map | rs121908871 |
PheGenI | rs121908871 |
Biobank | rs121908871 |
1000 genomes | rs121908871 |
hgdp | rs121908871 |
ensembl | rs121908871 |
geneview | rs121908871 |
scholar | rs121908871 |
rs121908871 | |
pharmgkb | rs121908871 |
gwascentral | rs121908871 |
openSNP | rs121908871 |
23andMe | rs121908871 |
SNPshot | rs121908871 |
SNPdbe | rs121908871 |
MSV3d | rs121908871 |
GWAS Ctlg | rs121908871 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121908871(G;G) |
Alt | rs121908871(G;G) |
Reference | Rs121908871(T;T) |
Significance | Pathogenic |
Disease | Hypothyroidism |
Variation | info |
Gene | LOC101928431 TSHR |
CLNDBN | Hypothyroidism, congenital, nongoitrous, 1 |
Reversed | 0 |
HGVS | NC_000014.8:g.81609572T>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000006814.4, |