rs55938914
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs55938914(-;-) |
Make rs55938914(-;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA) |
Make rs55938914(GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 19 |
Position | 45770231 |
Gene | DMPK, SIX5 |
is a | snp |
is | mentioned by |
dbSNP | rs55938914 |
dbSNP (classic) | rs55938914 |
ClinGen | rs55938914 |
ebi | rs55938914 |
HLI | rs55938914 |
Exac | rs55938914 |
Gnomad | rs55938914 |
Varsome | rs55938914 |
LitVar | rs55938914 |
Map | rs55938914 |
PheGenI | rs55938914 |
Biobank | rs55938914 |
1000 genomes | rs55938914 |
hgdp | rs55938914 |
ensembl | rs55938914 |
geneview | rs55938914 |
scholar | rs55938914 |
rs55938914 | |
pharmgkb | rs55938914 |
gwascentral | rs55938914 |
openSNP | rs55938914 |
23andMe | rs55938914 |
SNPshot | rs55938914 |
SNPdbe | rs55938914 |
MSV3d | rs55938914 |
GWAS Ctlg | rs55938914 |
Max Magnitude | 0 |
aka NM_001081560.2(DMPK):c.*224_*226CTG(51_?)
OMIM pathogenic variant