rs139365610
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs139365610(C;T) |
Make rs139365610(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 49807348 |
Gene | AP2A1, FUZ, LOC105372435 |
is a | snp |
is | mentioned by |
dbSNP | rs139365610 |
dbSNP (classic) | rs139365610 |
ClinGen | rs139365610 |
ebi | rs139365610 |
HLI | rs139365610 |
Exac | rs139365610 |
Gnomad | rs139365610 |
Varsome | rs139365610 |
LitVar | rs139365610 |
Map | rs139365610 |
PheGenI | rs139365610 |
Biobank | rs139365610 |
1000 genomes | rs139365610 |
hgdp | rs139365610 |
ensembl | rs139365610 |
geneview | rs139365610 |
scholar | rs139365610 |
rs139365610 | |
pharmgkb | rs139365610 |
gwascentral | rs139365610 |
openSNP | rs139365610 |
23andMe | rs139365610 |
SNPshot | rs139365610 |
SNPdbe | rs139365610 |
MSV3d | rs139365610 |
GWAS Ctlg | rs139365610 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs139365610(A;A) rs139365610(T;T) |
Alt | rs139365610(A;A) rs139365610(T;T) |
Reference | Rs139365610(C;C) |
Significance | Other |
Disease | Neural tube defects |
Variation | info |
Gene | FUZ AP2A1 |
CLNDBN | Neural tube defects, susceptibility to |
Reversed | 0 |
HGVS | NC_000019.9:g.50310605C>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000024614.4, |