rs200820631
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs200820631(C;T) |
Make rs200820631(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 8 |
Position | 73981293 |
Gene | TMEM70 |
is a | snp |
is | mentioned by |
dbSNP | rs200820631 |
dbSNP (classic) | rs200820631 |
ClinGen | rs200820631 |
ebi | rs200820631 |
HLI | rs200820631 |
Exac | rs200820631 |
Gnomad | rs200820631 |
Varsome | rs200820631 |
LitVar | rs200820631 |
Map | rs200820631 |
PheGenI | rs200820631 |
Biobank | rs200820631 |
1000 genomes | rs200820631 |
hgdp | rs200820631 |
ensembl | rs200820631 |
geneview | rs200820631 |
scholar | rs200820631 |
rs200820631 | |
pharmgkb | rs200820631 |
gwascentral | rs200820631 |
openSNP | rs200820631 |
23andMe | rs200820631 |
SNPshot | rs200820631 |
SNPdbe | rs200820631 |
MSV3d | rs200820631 |
GWAS Ctlg | rs200820631 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs200820631(T;T) |
Alt | rs200820631(T;T) |
Reference | Rs200820631(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TMEM70 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000008.10:g.74893528C>T |
CLNSRC | |
CLNACC | RCV000186210.1, |