rs1057518654
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1057518654(A;G) |
Make rs1057518654(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 13 |
Position | 110172721 |
Gene | COL4A1 |
is a | snp |
is | mentioned by |
dbSNP | rs1057518654 |
dbSNP (classic) | rs1057518654 |
ClinGen | rs1057518654 |
ebi | rs1057518654 |
HLI | rs1057518654 |
Exac | rs1057518654 |
Gnomad | rs1057518654 |
Varsome | rs1057518654 |
LitVar | rs1057518654 |
Map | rs1057518654 |
PheGenI | rs1057518654 |
Biobank | rs1057518654 |
1000 genomes | rs1057518654 |
hgdp | rs1057518654 |
ensembl | rs1057518654 |
geneview | rs1057518654 |
scholar | rs1057518654 |
rs1057518654 | |
pharmgkb | rs1057518654 |
gwascentral | rs1057518654 |
openSNP | rs1057518654 |
23andMe | rs1057518654 |
SNPshot | rs1057518654 |
SNPdbe | rs1057518654 |
MSV3d | rs1057518654 |
GWAS Ctlg | rs1057518654 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057518654(G;G) |
Alt | rs1057518654(G;G) |
Reference | Rs1057518654(A;A) |
Significance | Probable-Pathogenic |
Disease | Brain small vessel disease with hemorrhage |
Variation | info |
Gene | COL4A1 |
CLNDBN | Brain small vessel disease with hemorrhage |
Reversed | 1 |
HGVS | NC_000013.10:g.110825068T>C |
CLNSRC | |
CLNACC | RCV000414767.1, |