rs1864410
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1864410(A;A) |
Make rs1864410(A;C) |
Make rs1864410(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 43080177 |
Gene | RET |
is a | snp |
is | mentioned by |
dbSNP | rs1864410 |
dbSNP (classic) | rs1864410 |
ClinGen | rs1864410 |
ebi | rs1864410 |
HLI | rs1864410 |
Exac | rs1864410 |
Gnomad | rs1864410 |
Varsome | rs1864410 |
LitVar | rs1864410 |
Map | rs1864410 |
PheGenI | rs1864410 |
Biobank | rs1864410 |
1000 genomes | rs1864410 |
hgdp | rs1864410 |
ensembl | rs1864410 |
geneview | rs1864410 |
scholar | rs1864410 |
rs1864410 | |
pharmgkb | rs1864410 |
gwascentral | rs1864410 |
openSNP | rs1864410 |
23andMe | rs1864410 |
SNPshot | rs1864410 |
SNPdbe | rs1864410 |
MSV3d | rs1864410 |
GWAS Ctlg | rs1864410 |
Max Magnitude | 0 |
[PMID 24897126] RET Variants and Haplotype Analysis in a Cohort of Czech Patients with Hirschsprung Disease