rs113994115
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs113994115(G;T) |
Make rs113994115(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 15942281 |
Gene | MYCN, MYCNOS |
is a | snp |
is | mentioned by |
dbSNP | rs113994115 |
dbSNP (classic) | rs113994115 |
ClinGen | rs113994115 |
ebi | rs113994115 |
HLI | rs113994115 |
Exac | rs113994115 |
Gnomad | rs113994115 |
Varsome | rs113994115 |
LitVar | rs113994115 |
Map | rs113994115 |
PheGenI | rs113994115 |
Biobank | rs113994115 |
1000 genomes | rs113994115 |
hgdp | rs113994115 |
ensembl | rs113994115 |
geneview | rs113994115 |
scholar | rs113994115 |
rs113994115 | |
pharmgkb | rs113994115 |
gwascentral | rs113994115 |
openSNP | rs113994115 |
23andMe | rs113994115 |
SNPshot | rs113994115 |
SNPdbe | rs113994115 |
MSV3d | rs113994115 |
GWAS Ctlg | rs113994115 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs113994115(T;T) |
Alt | rs113994115(T;T) |
Reference | Rs113994115(G;G) |
Significance | Pathogenic |
Disease | Feingold syndrome 1 |
Variation | info |
Gene | MYCN MYCNOS |
CLNDBN | Feingold syndrome 1 |
Reversed | 0 |
HGVS | NC_000002.11:g.16082403G>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000014910.25, |