rs786204428
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CAGG;CAGG) | 0 | common in clinvar |
Make rs786204428(CAGG;TGTCCAAT) |
Make rs786204428(TGTCCAAT;TGTCCAAT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 150972557 |
Gene | CLRN1, CLRN1-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs786204428 |
dbSNP (classic) | rs786204428 |
ClinGen | rs786204428 |
ebi | rs786204428 |
HLI | rs786204428 |
Exac | rs786204428 |
Gnomad | rs786204428 |
Varsome | rs786204428 |
LitVar | rs786204428 |
Map | rs786204428 |
PheGenI | rs786204428 |
Biobank | rs786204428 |
1000 genomes | rs786204428 |
hgdp | rs786204428 |
ensembl | rs786204428 |
geneview | rs786204428 |
scholar | rs786204428 |
rs786204428 | |
pharmgkb | rs786204428 |
gwascentral | rs786204428 |
openSNP | rs786204428 |
23andMe | rs786204428 |
SNPshot | rs786204428 |
SNPdbe | rs786204428 |
MSV3d | rs786204428 |
GWAS Ctlg | rs786204428 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786204428(TGTCCAAT;TGTCCAAT) |
Alt | rs786204428(TGTCCAAT;TGTCCAAT) |
Reference | Rs786204428(CAGG;CAGG) |
Significance | Other |
Disease | Usher syndrome not provided |
Variation | info |
Gene | CLRN1-AS1 CLRN1 |
CLNDBN | Usher syndrome, type 3A not provided |
Reversed | 1 |
HGVS | NC_000003.11:g.150690344_150690347delCCTGinsATTGGACA |
CLNSRC | |
CLNACC | RCV000169027.2, RCV000478734.1, |