rs796051997
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs796051997(A;A) |
Make rs796051997(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 45508966 |
Gene | MMACHC |
is a | snp |
is | mentioned by |
dbSNP | rs796051997 |
dbSNP (classic) | rs796051997 |
ClinGen | rs796051997 |
ebi | rs796051997 |
HLI | rs796051997 |
Exac | rs796051997 |
Gnomad | rs796051997 |
Varsome | rs796051997 |
LitVar | rs796051997 |
Map | rs796051997 |
PheGenI | rs796051997 |
Biobank | rs796051997 |
1000 genomes | rs796051997 |
hgdp | rs796051997 |
ensembl | rs796051997 |
geneview | rs796051997 |
scholar | rs796051997 |
rs796051997 | |
pharmgkb | rs796051997 |
gwascentral | rs796051997 |
openSNP | rs796051997 |
23andMe | rs796051997 |
SNPshot | rs796051997 |
SNPdbe | rs796051997 |
MSV3d | rs796051997 |
GWAS Ctlg | rs796051997 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796051997(A;A) |
Alt | rs796051997(A;A) |
Reference | Rs796051997(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MMACHC |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.45974638G>A |
CLNSRC | |
CLNACC | RCV000186031.1, |