rs201824235
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs201824235(A;T) |
Make rs201824235(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 4 |
Position | 42963153 |
Gene | GRXCR1 |
is a | snp |
is | mentioned by |
dbSNP | rs201824235 |
dbSNP (classic) | rs201824235 |
ClinGen | rs201824235 |
ebi | rs201824235 |
HLI | rs201824235 |
Exac | rs201824235 |
Gnomad | rs201824235 |
Varsome | rs201824235 |
LitVar | rs201824235 |
Map | rs201824235 |
PheGenI | rs201824235 |
Biobank | rs201824235 |
1000 genomes | rs201824235 |
hgdp | rs201824235 |
ensembl | rs201824235 |
geneview | rs201824235 |
scholar | rs201824235 |
rs201824235 | |
pharmgkb | rs201824235 |
gwascentral | rs201824235 |
openSNP | rs201824235 |
23andMe | rs201824235 |
SNPshot | rs201824235 |
SNPdbe | rs201824235 |
MSV3d | rs201824235 |
GWAS Ctlg | rs201824235 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201824235(T;T) |
Alt | rs201824235(T;T) |
Reference | Rs201824235(A;A) |
Significance | Pathogenic |
Disease | Deafness |
Variation | info |
Gene | GRXCR1 |
CLNDBN | Deafness, autosomal recessive 25 |
Reversed | 0 |
HGVS | NC_000004.11:g.42965170A>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000000217.2, |