rs138834083
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs138834083(A;A) |
Make rs138834083(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 7223816 |
Gene | ACADVL, MIR324 |
is a | snp |
is | mentioned by |
dbSNP | rs138834083 |
dbSNP (classic) | rs138834083 |
ClinGen | rs138834083 |
ebi | rs138834083 |
HLI | rs138834083 |
Exac | rs138834083 |
Gnomad | rs138834083 |
Varsome | rs138834083 |
LitVar | rs138834083 |
Map | rs138834083 |
PheGenI | rs138834083 |
Biobank | rs138834083 |
1000 genomes | rs138834083 |
hgdp | rs138834083 |
ensembl | rs138834083 |
geneview | rs138834083 |
scholar | rs138834083 |
rs138834083 | |
pharmgkb | rs138834083 |
gwascentral | rs138834083 |
openSNP | rs138834083 |
23andMe | rs138834083 |
SNPshot | rs138834083 |
SNPdbe | rs138834083 |
MSV3d | rs138834083 |
GWAS Ctlg | rs138834083 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs138834083(A;A) |
Alt | rs138834083(A;A) |
Reference | Rs138834083(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | ACADVL MIR324 |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.7127135G>A |
CLNSRC | |
CLNACC | RCV000077902.5, RCV000418569.1, |