rs370356566
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs370356566(A;A) |
Make rs370356566(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 157471733 |
Gene | NIPAL4 |
is a | snp |
is | mentioned by |
dbSNP | rs370356566 |
dbSNP (classic) | rs370356566 |
ClinGen | rs370356566 |
ebi | rs370356566 |
HLI | rs370356566 |
Exac | rs370356566 |
Gnomad | rs370356566 |
Varsome | rs370356566 |
LitVar | rs370356566 |
Map | rs370356566 |
PheGenI | rs370356566 |
Biobank | rs370356566 |
1000 genomes | rs370356566 |
hgdp | rs370356566 |
ensembl | rs370356566 |
geneview | rs370356566 |
scholar | rs370356566 |
rs370356566 | |
pharmgkb | rs370356566 |
gwascentral | rs370356566 |
openSNP | rs370356566 |
23andMe | rs370356566 |
SNPshot | rs370356566 |
SNPdbe | rs370356566 |
MSV3d | rs370356566 |
GWAS Ctlg | rs370356566 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs370356566(A;A) |
Alt | rs370356566(A;A) |
Reference | Rs370356566(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ADAM19 NIPAL4 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.156898741G>A |
CLNSRC | |
CLNACC | RCV000414650.1, |