rs587776945
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs587776945(-;-) |
Make rs587776945(-;A) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 113100268 |
Gene | LRIG2 |
is a | snp |
is | mentioned by |
dbSNP | rs587776945 |
dbSNP (classic) | rs587776945 |
ClinGen | rs587776945 |
ebi | rs587776945 |
HLI | rs587776945 |
Exac | rs587776945 |
Gnomad | rs587776945 |
Varsome | rs587776945 |
LitVar | rs587776945 |
Map | rs587776945 |
PheGenI | rs587776945 |
Biobank | rs587776945 |
1000 genomes | rs587776945 |
hgdp | rs587776945 |
ensembl | rs587776945 |
geneview | rs587776945 |
scholar | rs587776945 |
rs587776945 | |
pharmgkb | rs587776945 |
gwascentral | rs587776945 |
openSNP | rs587776945 |
23andMe | rs587776945 |
SNPshot | rs587776945 |
SNPdbe | rs587776945 |
MSV3d | rs587776945 |
GWAS Ctlg | rs587776945 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587776945(-;-) |
Alt | rs587776945(-;-) |
Reference | Rs587776945(A;A) |
Significance | Pathogenic |
Disease | Urofacial syndrome 2 |
Variation | info |
Gene | LRIG2 |
CLNDBN | Urofacial syndrome 2 |
Reversed | 0 |
HGVS | NC_000001.10:g.113642890delA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000033224.5, |