rs750937323
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs750937323(A;G) |
Make rs750937323(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 15 |
Position | 68208178 |
Gene | CLN6 |
is a | snp |
is | mentioned by |
dbSNP | rs750937323 |
dbSNP (classic) | rs750937323 |
ClinGen | rs750937323 |
ebi | rs750937323 |
HLI | rs750937323 |
Exac | rs750937323 |
Gnomad | rs750937323 |
Varsome | rs750937323 |
LitVar | rs750937323 |
Map | rs750937323 |
PheGenI | rs750937323 |
Biobank | rs750937323 |
1000 genomes | rs750937323 |
hgdp | rs750937323 |
ensembl | rs750937323 |
geneview | rs750937323 |
scholar | rs750937323 |
rs750937323 | |
pharmgkb | rs750937323 |
gwascentral | rs750937323 |
openSNP | rs750937323 |
23andMe | rs750937323 |
SNPshot | rs750937323 |
SNPdbe | rs750937323 |
MSV3d | rs750937323 |
GWAS Ctlg | rs750937323 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs750937323(G;G) |
Alt | rs750937323(G;G) |
Reference | Rs750937323(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CLN6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.68500516A>G |
CLNSRC | |
CLNACC | RCV000416280.1, |