rs137957386
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs137957386(A;A) |
Make rs137957386(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 11027301 |
Gene | MASP2, TARDBP |
is a | snp |
is | mentioned by |
dbSNP | rs137957386 |
dbSNP (classic) | rs137957386 |
ClinGen | rs137957386 |
ebi | rs137957386 |
HLI | rs137957386 |
Exac | rs137957386 |
Gnomad | rs137957386 |
Varsome | rs137957386 |
LitVar | rs137957386 |
Map | rs137957386 |
PheGenI | rs137957386 |
Biobank | rs137957386 |
1000 genomes | rs137957386 |
hgdp | rs137957386 |
ensembl | rs137957386 |
geneview | rs137957386 |
scholar | rs137957386 |
rs137957386 | |
pharmgkb | rs137957386 |
gwascentral | rs137957386 |
openSNP | rs137957386 |
23andMe | rs137957386 |
SNPshot | rs137957386 |
SNPdbe | rs137957386 |
MSV3d | rs137957386 |
GWAS Ctlg | rs137957386 |
Max Magnitude | 0 |
[PMID 21499247] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
ClinVar | |
---|---|
Risk | rs137957386(A;A) rs137957386(C;C) |
Alt | rs137957386(A;A) rs137957386(C;C) |
Reference | Rs137957386(T;T) |
Significance | Untested |
Disease | Malignant melanoma |
Variation | info |
Gene | MASP2 |
CLNDBN | Malignant melanoma |
Reversed | 0 |
HGVS | NC_000001.11:g.11027301T>A |
CLNSRC | ClinVar |
CLNACC | RCV000059831.2, |