rs750614500
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs750614500(C;T) |
Make rs750614500(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 22 |
Position | 40358949 |
Gene | ADSL |
is a | snp |
is | mentioned by |
dbSNP | rs750614500 |
dbSNP (classic) | rs750614500 |
ClinGen | rs750614500 |
ebi | rs750614500 |
HLI | rs750614500 |
Exac | rs750614500 |
Gnomad | rs750614500 |
Varsome | rs750614500 |
LitVar | rs750614500 |
Map | rs750614500 |
PheGenI | rs750614500 |
Biobank | rs750614500 |
1000 genomes | rs750614500 |
hgdp | rs750614500 |
ensembl | rs750614500 |
geneview | rs750614500 |
scholar | rs750614500 |
rs750614500 | |
pharmgkb | rs750614500 |
gwascentral | rs750614500 |
openSNP | rs750614500 |
23andMe | rs750614500 |
SNPshot | rs750614500 |
SNPdbe | rs750614500 |
MSV3d | rs750614500 |
GWAS Ctlg | rs750614500 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs750614500(T;T) |
Alt | rs750614500(T;T) |
Reference | Rs750614500(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ADSL |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000022.10:g.40754953C>T |
CLNSRC | |
CLNACC | RCV000186710.1, |