rs757318536
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs757318536(C;T) |
Make rs757318536(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 150553240 |
Gene | ADAMTSL4, LOC100289061 |
is a | snp |
is | mentioned by |
dbSNP | rs757318536 |
dbSNP (classic) | rs757318536 |
ClinGen | rs757318536 |
ebi | rs757318536 |
HLI | rs757318536 |
Exac | rs757318536 |
Gnomad | rs757318536 |
Varsome | rs757318536 |
LitVar | rs757318536 |
Map | rs757318536 |
PheGenI | rs757318536 |
Biobank | rs757318536 |
1000 genomes | rs757318536 |
hgdp | rs757318536 |
ensembl | rs757318536 |
geneview | rs757318536 |
scholar | rs757318536 |
rs757318536 | |
pharmgkb | rs757318536 |
gwascentral | rs757318536 |
openSNP | rs757318536 |
23andMe | rs757318536 |
SNPshot | rs757318536 |
SNPdbe | rs757318536 |
MSV3d | rs757318536 |
GWAS Ctlg | rs757318536 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs757318536(T;T) |
Alt | rs757318536(T;T) |
Reference | Rs757318536(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ADAMTSL4 LOC100289061 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.150525716C>T |
CLNSRC | |
CLNACC | RCV000440699.1, |