rs121912692
From SNPedia
Merged into | rs121912691 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs121912692(A;A) |
Make rs121912692(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 44312653 |
Gene | SLC3A1 |
is a | snp |
is | mentioned by |
dbSNP | rs121912692 |
dbSNP (classic) | rs121912692 |
ClinGen | rs121912692 |
ebi | rs121912692 |
HLI | rs121912692 |
Exac | rs121912692 |
Gnomad | rs121912692 |
Varsome | rs121912692 |
LitVar | rs121912692 |
Map | rs121912692 |
PheGenI | rs121912692 |
Biobank | rs121912692 |
1000 genomes | rs121912692 |
hgdp | rs121912692 |
ensembl | rs121912692 |
geneview | rs121912692 |
scholar | rs121912692 |
rs121912692 | |
pharmgkb | rs121912692 |
gwascentral | rs121912692 |
openSNP | rs121912692 |
23andMe | rs121912692 |
SNPshot | rs121912692 |
SNPdbe | rs121912692 |
MSV3d | rs121912692 |
GWAS Ctlg | rs121912692 |
Status | Merged into rs121912691 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121912692(A;A) |
Alt | rs121912692(A;A) |
Reference | Rs121912692(T;T) |
Significance | Pathogenic |
Disease | Cystinuria |
Variation | info |
Gene | SLC3A1 |
CLNDBN | Cystinuria |
Reversed | 0 |
HGVS | NC_000002.11:g.44539792T>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | SCV000040042.1, |