rs1060499754
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1060499754(A;G) |
Make rs1060499754(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 19797472 |
Gene | ULK2 |
is a | snp |
is | mentioned by |
dbSNP | rs1060499754 |
dbSNP (classic) | rs1060499754 |
ClinGen | rs1060499754 |
ebi | rs1060499754 |
HLI | rs1060499754 |
Exac | rs1060499754 |
Gnomad | rs1060499754 |
Varsome | rs1060499754 |
LitVar | rs1060499754 |
Map | rs1060499754 |
PheGenI | rs1060499754 |
Biobank | rs1060499754 |
1000 genomes | rs1060499754 |
hgdp | rs1060499754 |
ensembl | rs1060499754 |
geneview | rs1060499754 |
scholar | rs1060499754 |
rs1060499754 | |
pharmgkb | rs1060499754 |
gwascentral | rs1060499754 |
openSNP | rs1060499754 |
23andMe | rs1060499754 |
SNPshot | rs1060499754 |
SNPdbe | rs1060499754 |
MSV3d | rs1060499754 |
GWAS Ctlg | rs1060499754 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1060499754(G;G) |
Alt | rs1060499754(G;G) |
Reference | Rs1060499754(A;A) |
Significance | Probable-Pathogenic |
Disease | Abnormality of brain morphology |
Variation | info |
Gene | ULK2 |
CLNDBN | Abnormality of brain morphology |
Reversed | 1 |
HGVS | NC_000017.10:g.19700785T>C |
CLNSRC | |
CLNACC | RCV000454305.1, |