rs1064797340
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Chromosome | 7 |
Position | 107672192 |
Gene | SLC26A4 |
is a | snp |
is | mentioned by |
dbSNP | rs1064797340 |
dbSNP (classic) | rs1064797340 |
ClinGen | rs1064797340 |
ebi | rs1064797340 |
HLI | rs1064797340 |
Exac | rs1064797340 |
Gnomad | rs1064797340 |
Varsome | rs1064797340 |
LitVar | rs1064797340 |
Map | rs1064797340 |
PheGenI | rs1064797340 |
Biobank | rs1064797340 |
1000 genomes | rs1064797340 |
hgdp | rs1064797340 |
ensembl | rs1064797340 |
geneview | rs1064797340 |
scholar | rs1064797340 |
rs1064797340 | |
pharmgkb | rs1064797340 |
gwascentral | rs1064797340 |
openSNP | rs1064797340 |
23andMe | rs1064797340 |
SNPshot | rs1064797340 |
SNPdbe | rs1064797340 |
MSV3d | rs1064797340 |
GWAS Ctlg | rs1064797340 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064797340(T;T) |
Alt | rs1064797340(T;T) |
Reference | Rs1064797340(-;-) |
Significance | Probable-Pathogenic |
Disease | Pendred's syndrome not provided |
Variation | info |
Gene | SLC26A4 |
CLNDBN | Pendred's syndrome not provided |
Reversed | 0 |
HGVS | NC_000007.13:g.107312643dupT |
CLNSRC | |
CLNACC | RCV000169571.1, RCV000488403.1, |