rs730880504
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs730880504(A;A) |
Make rs730880504(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 15 |
Position | 66436866 |
Gene | MAP2K1 |
is a | snp |
is | mentioned by |
dbSNP | rs730880504 |
dbSNP (classic) | rs730880504 |
ClinGen | rs730880504 |
ebi | rs730880504 |
HLI | rs730880504 |
Exac | rs730880504 |
Gnomad | rs730880504 |
Varsome | rs730880504 |
LitVar | rs730880504 |
Map | rs730880504 |
PheGenI | rs730880504 |
Biobank | rs730880504 |
1000 genomes | rs730880504 |
hgdp | rs730880504 |
ensembl | rs730880504 |
geneview | rs730880504 |
scholar | rs730880504 |
rs730880504 | |
pharmgkb | rs730880504 |
gwascentral | rs730880504 |
openSNP | rs730880504 |
23andMe | rs730880504 |
SNPshot | rs730880504 |
SNPdbe | rs730880504 |
MSV3d | rs730880504 |
GWAS Ctlg | rs730880504 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730880504(A;A) |
Alt | rs730880504(A;A) |
Reference | Rs730880504(G;G) |
Significance | Pathogenic |
Disease | not specified |
Variation | info |
Gene | MAP2K1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000015.9:g.66729204G>A |
CLNSRC | |
CLNACC | RCV000158009.2, |