rs377731205
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs377731205(C;T) |
Make rs377731205(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 19 |
Position | 36097074 |
Gene | WDR62 |
is a | snp |
is | mentioned by |
dbSNP | rs377731205 |
dbSNP (classic) | rs377731205 |
ClinGen | rs377731205 |
ebi | rs377731205 |
HLI | rs377731205 |
Exac | rs377731205 |
Gnomad | rs377731205 |
Varsome | rs377731205 |
LitVar | rs377731205 |
Map | rs377731205 |
PheGenI | rs377731205 |
Biobank | rs377731205 |
1000 genomes | rs377731205 |
hgdp | rs377731205 |
ensembl | rs377731205 |
geneview | rs377731205 |
scholar | rs377731205 |
rs377731205 | |
pharmgkb | rs377731205 |
gwascentral | rs377731205 |
openSNP | rs377731205 |
23andMe | rs377731205 |
SNPshot | rs377731205 |
SNPdbe | rs377731205 |
MSV3d | rs377731205 |
GWAS Ctlg | rs377731205 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs377731205(T;T) |
Alt | rs377731205(T;T) |
Reference | Rs377731205(C;C) |
Significance | Pathogenic |
Disease | Abnormality of neuronal migration |
Variation | info |
Gene | WDR62 |
CLNDBN | Abnormality of neuronal migration |
Reversed | 0 |
HGVS | NC_000019.9:g.36587976C>T |
CLNSRC | |
CLNACC | RCV000201333.1, |