rs267607167
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs267607167(C;T) |
Make rs267607167(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 160421171 |
Gene | VANGL2 |
is a | snp |
is | mentioned by |
dbSNP | rs267607167 |
dbSNP (classic) | rs267607167 |
ClinGen | rs267607167 |
ebi | rs267607167 |
HLI | rs267607167 |
Exac | rs267607167 |
Gnomad | rs267607167 |
Varsome | rs267607167 |
LitVar | rs267607167 |
Map | rs267607167 |
PheGenI | rs267607167 |
Biobank | rs267607167 |
1000 genomes | rs267607167 |
hgdp | rs267607167 |
ensembl | rs267607167 |
geneview | rs267607167 |
scholar | rs267607167 |
rs267607167 | |
pharmgkb | rs267607167 |
gwascentral | rs267607167 |
openSNP | rs267607167 |
23andMe | rs267607167 |
SNPshot | rs267607167 |
SNPdbe | rs267607167 |
MSV3d | rs267607167 |
GWAS Ctlg | rs267607167 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs267607167(G;G) rs267607167(T;T) |
Alt | rs267607167(G;G) rs267607167(T;T) |
Reference | Rs267607167(C;C) |
Significance | Other |
Disease | Neural tube defects |
Variation | info |
Gene | VANGL2 |
CLNDBN | Neural tube defects, susceptibility to |
Reversed | 0 |
HGVS | NC_000001.10:g.160390961C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000009619.7, |