rs587777234
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs587777234(G;G) |
Make rs587777234(G;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 6 |
Position | 12293956 |
Gene | EDN1 |
is a | snp |
is | mentioned by |
dbSNP | rs587777234 |
dbSNP (classic) | rs587777234 |
ClinGen | rs587777234 |
ebi | rs587777234 |
HLI | rs587777234 |
Exac | rs587777234 |
Gnomad | rs587777234 |
Varsome | rs587777234 |
LitVar | rs587777234 |
Map | rs587777234 |
PheGenI | rs587777234 |
Biobank | rs587777234 |
1000 genomes | rs587777234 |
hgdp | rs587777234 |
ensembl | rs587777234 |
geneview | rs587777234 |
scholar | rs587777234 |
rs587777234 | |
pharmgkb | rs587777234 |
gwascentral | rs587777234 |
openSNP | rs587777234 |
23andMe | rs587777234 |
SNPshot | rs587777234 |
SNPdbe | rs587777234 |
MSV3d | rs587777234 |
GWAS Ctlg | rs587777234 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587777234(G;G) |
Alt | rs587777234(G;G) |
Reference | Rs587777234(T;T) |
Significance | Pathogenic |
Disease | Question mark ears |
Variation | info |
Gene | EDN1 |
CLNDBN | Question mark ears, isolated |
Reversed | 0 |
HGVS | NC_000006.11:g.12294189T>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000106315.3, |