rs1064797138
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Chromosome | 1 |
Position | 216207368 |
Gene | LOC105372918, USH2A |
is a | snp |
is | mentioned by |
dbSNP | rs1064797138 |
dbSNP (classic) | rs1064797138 |
ClinGen | rs1064797138 |
ebi | rs1064797138 |
HLI | rs1064797138 |
Exac | rs1064797138 |
Gnomad | rs1064797138 |
Varsome | rs1064797138 |
LitVar | rs1064797138 |
Map | rs1064797138 |
PheGenI | rs1064797138 |
Biobank | rs1064797138 |
1000 genomes | rs1064797138 |
hgdp | rs1064797138 |
ensembl | rs1064797138 |
geneview | rs1064797138 |
scholar | rs1064797138 |
rs1064797138 | |
pharmgkb | rs1064797138 |
gwascentral | rs1064797138 |
openSNP | rs1064797138 |
23andMe | rs1064797138 |
SNPshot | rs1064797138 |
SNPdbe | rs1064797138 |
MSV3d | rs1064797138 |
GWAS Ctlg | rs1064797138 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064797138(A;A) |
Alt | rs1064797138(A;A) |
Reference | Rs1064797138(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | USH2A |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000001.10:g.216380710C>T |
CLNSRC | |
CLNACC | RCV000488319.1, |