rs387906297
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AGTT;AGTT) | 0 | common in clinvar |
(TTAG;TTAG) | 0 | common in clinvar |
Make rs387906297(-;-) |
Make rs387906297(-;TTAG) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 75761278 |
Gene | ACADM |
is a | snp |
is | mentioned by |
dbSNP | rs387906297 |
dbSNP (classic) | rs387906297 |
ClinGen | rs387906297 |
ebi | rs387906297 |
HLI | rs387906297 |
Exac | rs387906297 |
Gnomad | rs387906297 |
Varsome | rs387906297 |
LitVar | rs387906297 |
Map | rs387906297 |
PheGenI | rs387906297 |
Biobank | rs387906297 |
1000 genomes | rs387906297 |
hgdp | rs387906297 |
ensembl | rs387906297 |
geneview | rs387906297 |
scholar | rs387906297 |
rs387906297 | |
pharmgkb | rs387906297 |
gwascentral | rs387906297 |
openSNP | rs387906297 |
23andMe | rs387906297 |
SNPshot | rs387906297 |
SNPdbe | rs387906297 |
MSV3d | rs387906297 |
GWAS Ctlg | rs387906297 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387906297(-;-) |
Alt | rs387906297(-;-) |
Reference | Rs387906297(AGTT;AGTT) |
Significance | Pathogenic |
Disease | Medium-chain acyl-coenzyme A dehydrogenase deficiency not provided |
Variation | info |
Gene | ACADM |
CLNDBN | Medium-chain acyl-coenzyme A dehydrogenase deficiency not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.76226963_76226966delTTAG |
CLNSRC | HGMD OMIM Allelic Variant |
CLNACC | RCV000003775.2, RCV000077877.3, |