rs1057524702
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1057524702(G;T) |
Make rs1057524702(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 155237480 |
Gene | GBA |
is a | snp |
is | mentioned by |
dbSNP | rs1057524702 |
dbSNP (classic) | rs1057524702 |
ClinGen | rs1057524702 |
ebi | rs1057524702 |
HLI | rs1057524702 |
Exac | rs1057524702 |
Gnomad | rs1057524702 |
Varsome | rs1057524702 |
LitVar | rs1057524702 |
Map | rs1057524702 |
PheGenI | rs1057524702 |
Biobank | rs1057524702 |
1000 genomes | rs1057524702 |
hgdp | rs1057524702 |
ensembl | rs1057524702 |
geneview | rs1057524702 |
scholar | rs1057524702 |
rs1057524702 | |
pharmgkb | rs1057524702 |
gwascentral | rs1057524702 |
openSNP | rs1057524702 |
23andMe | rs1057524702 |
SNPshot | rs1057524702 |
SNPdbe | rs1057524702 |
MSV3d | rs1057524702 |
GWAS Ctlg | rs1057524702 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057524702(T;T) |
Alt | rs1057524702(T;T) |
Reference | Rs1057524702(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GBA |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000001.10:g.155207271C>A |
CLNSRC | |
CLNACC | RCV000443344.1, |