rs786201013
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs786201013(A;T) |
Make rs786201013(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 200603922 |
Gene | KIF14 |
is a | snp |
is | mentioned by |
dbSNP | rs786201013 |
dbSNP (classic) | rs786201013 |
ClinGen | rs786201013 |
ebi | rs786201013 |
HLI | rs786201013 |
Exac | rs786201013 |
Gnomad | rs786201013 |
Varsome | rs786201013 |
LitVar | rs786201013 |
Map | rs786201013 |
PheGenI | rs786201013 |
Biobank | rs786201013 |
1000 genomes | rs786201013 |
hgdp | rs786201013 |
ensembl | rs786201013 |
geneview | rs786201013 |
scholar | rs786201013 |
rs786201013 | |
pharmgkb | rs786201013 |
gwascentral | rs786201013 |
openSNP | rs786201013 |
23andMe | rs786201013 |
SNPshot | rs786201013 |
SNPdbe | rs786201013 |
MSV3d | rs786201013 |
GWAS Ctlg | rs786201013 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786201013(T;T) |
Alt | rs786201013(T;T) |
Reference | Rs786201013(A;A) |
Significance | Pathogenic |
Disease | Meckel syndrome 12 |
Variation | info |
Gene | KIF14 |
CLNDBN | Meckel syndrome 12 |
Reversed | 1 |
HGVS | NC_000001.10:g.200573050T>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000162211.3, |