rs141823837
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs141823837(C;T) |
Make rs141823837(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 94060739 |
Gene | ABCA4 |
is a | snp |
is | mentioned by |
dbSNP | rs141823837 |
dbSNP (classic) | rs141823837 |
ClinGen | rs141823837 |
ebi | rs141823837 |
HLI | rs141823837 |
Exac | rs141823837 |
Gnomad | rs141823837 |
Varsome | rs141823837 |
LitVar | rs141823837 |
Map | rs141823837 |
PheGenI | rs141823837 |
Biobank | rs141823837 |
1000 genomes | rs141823837 |
hgdp | rs141823837 |
ensembl | rs141823837 |
geneview | rs141823837 |
scholar | rs141823837 |
rs141823837 | |
pharmgkb | rs141823837 |
gwascentral | rs141823837 |
openSNP | rs141823837 |
23andMe | rs141823837 |
SNPshot | rs141823837 |
SNPdbe | rs141823837 |
MSV3d | rs141823837 |
GWAS Ctlg | rs141823837 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs141823837(T;T) |
Alt | rs141823837(T;T) |
Reference | Rs141823837(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCA4 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.94526295C>T |
CLNSRC | |
CLNACC | RCV000484928.1, |