rs145734330
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs145734330(A;A) |
Make rs145734330(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 15930681 |
Gene | SPEN |
is a | snp |
is | mentioned by |
dbSNP | rs145734330 |
dbSNP (classic) | rs145734330 |
ClinGen | rs145734330 |
ebi | rs145734330 |
HLI | rs145734330 |
Exac | rs145734330 |
Gnomad | rs145734330 |
Varsome | rs145734330 |
LitVar | rs145734330 |
Map | rs145734330 |
PheGenI | rs145734330 |
Biobank | rs145734330 |
1000 genomes | rs145734330 |
hgdp | rs145734330 |
ensembl | rs145734330 |
geneview | rs145734330 |
scholar | rs145734330 |
rs145734330 | |
pharmgkb | rs145734330 |
gwascentral | rs145734330 |
openSNP | rs145734330 |
23andMe | rs145734330 |
SNPshot | rs145734330 |
SNPdbe | rs145734330 |
MSV3d | rs145734330 |
GWAS Ctlg | rs145734330 |
Max Magnitude | 0 |
[PMID 21499247] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
ClinVar | |
---|---|
Risk | rs145734330(A;A) |
Alt | rs145734330(A;A) |
Reference | Rs145734330(G;G) |
Significance | Untested |
Disease | Malignant melanoma |
Variation | info |
Gene | SPEN |
CLNDBN | Malignant melanoma |
Reversed | 0 |
HGVS | NC_000001.11:g.15930681G>A |
CLNSRC | ClinVar |
CLNACC | RCV000059971.2, |