rs574376340
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs574376340(A;A) |
Make rs574376340(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 50168529 |
Gene | LOC105371818, SGCA |
is a | snp |
is | mentioned by |
dbSNP | rs574376340 |
dbSNP (classic) | rs574376340 |
ClinGen | rs574376340 |
ebi | rs574376340 |
HLI | rs574376340 |
Exac | rs574376340 |
Gnomad | rs574376340 |
Varsome | rs574376340 |
LitVar | rs574376340 |
Map | rs574376340 |
PheGenI | rs574376340 |
Biobank | rs574376340 |
1000 genomes | rs574376340 |
hgdp | rs574376340 |
ensembl | rs574376340 |
geneview | rs574376340 |
scholar | rs574376340 |
rs574376340 | |
pharmgkb | rs574376340 |
gwascentral | rs574376340 |
openSNP | rs574376340 |
23andMe | rs574376340 |
SNPshot | rs574376340 |
SNPdbe | rs574376340 |
MSV3d | rs574376340 |
GWAS Ctlg | rs574376340 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs574376340(A;A) rs574376340(T;T) |
Alt | rs574376340(A;A) rs574376340(T;T) |
Reference | Rs574376340(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | SGCA |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.48245890C>A |
CLNSRC | |
CLNACC | RCV000377081.1, RCV000486077.1, |