rs137853198
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs137853198(A;A) |
Make rs137853198(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 77942632 |
Gene | NEXN |
is a | snp |
is | mentioned by |
dbSNP | rs137853198 |
dbSNP (classic) | rs137853198 |
ClinGen | rs137853198 |
ebi | rs137853198 |
HLI | rs137853198 |
Exac | rs137853198 |
Gnomad | rs137853198 |
Varsome | rs137853198 |
LitVar | rs137853198 |
Map | rs137853198 |
PheGenI | rs137853198 |
Biobank | rs137853198 |
1000 genomes | rs137853198 |
hgdp | rs137853198 |
ensembl | rs137853198 |
geneview | rs137853198 |
scholar | rs137853198 |
rs137853198 | |
pharmgkb | rs137853198 |
gwascentral | rs137853198 |
openSNP | rs137853198 |
23andMe | rs137853198 |
SNPshot | rs137853198 |
SNPdbe | rs137853198 |
MSV3d | rs137853198 |
GWAS Ctlg | rs137853198 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137853198(A;A) |
Alt | rs137853198(A;A) |
Reference | Rs137853198(C;C) |
Significance | Pathogenic |
Disease | Dilated cardiomyopathy 1CC |
Variation | info |
Gene | NEXN |
CLNDBN | Dilated cardiomyopathy 1CC |
Reversed | 0 |
HGVS | NC_000001.10:g.78408317C>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000000355.3, |