rs373551988
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs373551988(A;A) |
Make rs373551988(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 133353855 |
Gene | SURF1 |
is a | snp |
is | mentioned by |
dbSNP | rs373551988 |
dbSNP (classic) | rs373551988 |
ClinGen | rs373551988 |
ebi | rs373551988 |
HLI | rs373551988 |
Exac | rs373551988 |
Gnomad | rs373551988 |
Varsome | rs373551988 |
LitVar | rs373551988 |
Map | rs373551988 |
PheGenI | rs373551988 |
Biobank | rs373551988 |
1000 genomes | rs373551988 |
hgdp | rs373551988 |
ensembl | rs373551988 |
geneview | rs373551988 |
scholar | rs373551988 |
rs373551988 | |
pharmgkb | rs373551988 |
gwascentral | rs373551988 |
openSNP | rs373551988 |
23andMe | rs373551988 |
SNPshot | rs373551988 |
SNPdbe | rs373551988 |
MSV3d | rs373551988 |
GWAS Ctlg | rs373551988 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs373551988(A;A) |
Alt | rs373551988(A;A) |
Reference | Rs373551988(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SURF1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.136220710G>A |
CLNSRC | |
CLNACC | RCV000200389.1, |