rs137853307
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs137853307(C;G) |
| Make rs137853307(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 35684765 |
| Gene | TPM2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs137853307 |
| dbSNP (classic) | rs137853307 |
| ClinGen | rs137853307 |
| ebi | rs137853307 |
| HLI | rs137853307 |
| Exac | rs137853307 |
| Gnomad | rs137853307 |
| Varsome | rs137853307 |
| LitVar | rs137853307 |
| Map | rs137853307 |
| PheGenI | rs137853307 |
| Biobank | rs137853307 |
| 1000 genomes | rs137853307 |
| hgdp | rs137853307 |
| ensembl | rs137853307 |
| geneview | rs137853307 |
| scholar | rs137853307 |
| rs137853307 | |
| pharmgkb | rs137853307 |
| gwascentral | rs137853307 |
| openSNP | rs137853307 |
| 23andMe | rs137853307 |
| SNPshot | rs137853307 |
| SNPdbe | rs137853307 |
| MSV3d | rs137853307 |
| GWAS Ctlg | rs137853307 |
| Max Magnitude | 0 |
Nemaline myopathy; NEM4
OMIM 190990.0008
| ClinVar | |
|---|---|
| Risk | rs137853307(G;G) |
| Alt | rs137853307(G;G) |
| Reference | Rs137853307(C;C) |
| Significance | Pathogenic |
| Disease | Cap myopathy 2 not provided |
| Variation | info |
| Gene | TPM2 |
| CLNDBN | Cap myopathy 2 not provided |
| Reversed | 1 |
| HGVS | NC_000009.11:g.35684762G>C |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000013283.19, RCV000128687.1, |
[PMID 19047562] New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutations.
