rs794729179
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs794729179(A;A) |
Make rs794729179(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 14141692 |
Gene | TMEM43 |
is a | snp |
is | mentioned by |
dbSNP | rs794729179 |
dbSNP (classic) | rs794729179 |
ClinGen | rs794729179 |
ebi | rs794729179 |
HLI | rs794729179 |
Exac | rs794729179 |
Gnomad | rs794729179 |
Varsome | rs794729179 |
LitVar | rs794729179 |
Map | rs794729179 |
PheGenI | rs794729179 |
Biobank | rs794729179 |
1000 genomes | rs794729179 |
hgdp | rs794729179 |
ensembl | rs794729179 |
geneview | rs794729179 |
scholar | rs794729179 |
rs794729179 | |
pharmgkb | rs794729179 |
gwascentral | rs794729179 |
openSNP | rs794729179 |
23andMe | rs794729179 |
SNPshot | rs794729179 |
SNPdbe | rs794729179 |
MSV3d | rs794729179 |
GWAS Ctlg | rs794729179 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794729179(A;A) |
Alt | rs794729179(A;A) |
Reference | Rs794729179(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TMEM43 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.14183192G>A |
CLNSRC | |
CLNACC | RCV000183945.2, |