rs29001611
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs29001611(A;G) |
Make rs29001611(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 47630754 |
Gene | TPMTP1 |
is a | snp |
is | mentioned by |
dbSNP | rs29001611 |
dbSNP (classic) | rs29001611 |
ClinGen | rs29001611 |
ebi | rs29001611 |
HLI | rs29001611 |
Exac | rs29001611 |
Gnomad | rs29001611 |
Varsome | rs29001611 |
LitVar | rs29001611 |
Map | rs29001611 |
PheGenI | rs29001611 |
Biobank | rs29001611 |
1000 genomes | rs29001611 |
hgdp | rs29001611 |
ensembl | rs29001611 |
geneview | rs29001611 |
scholar | rs29001611 |
rs29001611 | |
pharmgkb | rs29001611 |
gwascentral | rs29001611 |
openSNP | rs29001611 |
23andMe | rs29001611 |
SNPshot | rs29001611 |
SNPdbe | rs29001611 |
MSV3d | rs29001611 |
GWAS Ctlg | rs29001611 |
Max Magnitude | 0 |
Far away from the other TPMT snps, this one comes from OMIM. dbSNP's geneview suggests that (G) should be normal, and (A) should be variant, but based this on "no gene model". 23andMe doesn't seem to actually be reporting this snp any longer.