rs757052602
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs757052602(A;T) |
Make rs757052602(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 71641068 |
Gene | MCCC2 |
is a | snp |
is | mentioned by |
dbSNP | rs757052602 |
dbSNP (classic) | rs757052602 |
ClinGen | rs757052602 |
ebi | rs757052602 |
HLI | rs757052602 |
Exac | rs757052602 |
Gnomad | rs757052602 |
Varsome | rs757052602 |
LitVar | rs757052602 |
Map | rs757052602 |
PheGenI | rs757052602 |
Biobank | rs757052602 |
1000 genomes | rs757052602 |
hgdp | rs757052602 |
ensembl | rs757052602 |
geneview | rs757052602 |
scholar | rs757052602 |
rs757052602 | |
pharmgkb | rs757052602 |
gwascentral | rs757052602 |
openSNP | rs757052602 |
23andMe | rs757052602 |
SNPshot | rs757052602 |
SNPdbe | rs757052602 |
MSV3d | rs757052602 |
GWAS Ctlg | rs757052602 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs757052602(T;T) |
Alt | rs757052602(T;T) |
Reference | Rs757052602(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MCCC2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.70936895A>T |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000186003.3, |