rs863223962
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs863223962(C;T) |
Make rs863223962(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 206767375 |
Gene | FASTKD2, MDH1B |
is a | snp |
is | mentioned by |
dbSNP | rs863223962 |
dbSNP (classic) | rs863223962 |
ClinGen | rs863223962 |
ebi | rs863223962 |
HLI | rs863223962 |
Exac | rs863223962 |
Gnomad | rs863223962 |
Varsome | rs863223962 |
LitVar | rs863223962 |
Map | rs863223962 |
PheGenI | rs863223962 |
Biobank | rs863223962 |
1000 genomes | rs863223962 |
hgdp | rs863223962 |
ensembl | rs863223962 |
geneview | rs863223962 |
scholar | rs863223962 |
rs863223962 | |
pharmgkb | rs863223962 |
gwascentral | rs863223962 |
openSNP | rs863223962 |
23andMe | rs863223962 |
SNPshot | rs863223962 |
SNPdbe | rs863223962 |
MSV3d | rs863223962 |
GWAS Ctlg | rs863223962 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863223962(T;T) |
Alt | rs863223962(T;T) |
Reference | Rs863223962(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | FASTKD2 MDH1B |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.207632099C>T |
CLNSRC | |
CLNACC | RCV000198572.2, |