rs371410845
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs371410845(A;A) |
Make rs371410845(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 229432575 |
Gene | ACTA1 |
is a | snp |
is | mentioned by |
dbSNP | rs371410845 |
dbSNP (classic) | rs371410845 |
ClinGen | rs371410845 |
ebi | rs371410845 |
HLI | rs371410845 |
Exac | rs371410845 |
Gnomad | rs371410845 |
Varsome | rs371410845 |
LitVar | rs371410845 |
Map | rs371410845 |
PheGenI | rs371410845 |
Biobank | rs371410845 |
1000 genomes | rs371410845 |
hgdp | rs371410845 |
ensembl | rs371410845 |
geneview | rs371410845 |
scholar | rs371410845 |
rs371410845 | |
pharmgkb | rs371410845 |
gwascentral | rs371410845 |
openSNP | rs371410845 |
23andMe | rs371410845 |
SNPshot | rs371410845 |
SNPdbe | rs371410845 |
MSV3d | rs371410845 |
GWAS Ctlg | rs371410845 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs371410845(A;A) rs371410845(T;T) |
Alt | rs371410845(A;A) rs371410845(T;T) |
Reference | Rs371410845(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACTA1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.229568322G>T |
CLNSRC | |
CLNACC | RCV000261100.1, |