rs781948238
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs781948238(A;A) |
Make rs781948238(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 133354823 |
Gene | SURF1, SURF2 |
is a | snp |
is | mentioned by |
dbSNP | rs781948238 |
dbSNP (classic) | rs781948238 |
ClinGen | rs781948238 |
ebi | rs781948238 |
HLI | rs781948238 |
Exac | rs781948238 |
Gnomad | rs781948238 |
Varsome | rs781948238 |
LitVar | rs781948238 |
Map | rs781948238 |
PheGenI | rs781948238 |
Biobank | rs781948238 |
1000 genomes | rs781948238 |
hgdp | rs781948238 |
ensembl | rs781948238 |
geneview | rs781948238 |
scholar | rs781948238 |
rs781948238 | |
pharmgkb | rs781948238 |
gwascentral | rs781948238 |
openSNP | rs781948238 |
23andMe | rs781948238 |
SNPshot | rs781948238 |
SNPdbe | rs781948238 |
MSV3d | rs781948238 |
GWAS Ctlg | rs781948238 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs781948238(A;A) |
Alt | rs781948238(A;A) |
Reference | Rs781948238(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SURF2 SURF1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.136221678C>A |
CLNSRC | |
CLNACC | RCV000422985.1, |