rs397517918
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs397517918(A;A) |
Make rs397517918(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 71215405 |
Gene | EYA1 |
is a | snp |
is | mentioned by |
dbSNP | rs397517918 |
dbSNP (classic) | rs397517918 |
ClinGen | rs397517918 |
ebi | rs397517918 |
HLI | rs397517918 |
Exac | rs397517918 |
Gnomad | rs397517918 |
Varsome | rs397517918 |
LitVar | rs397517918 |
Map | rs397517918 |
PheGenI | rs397517918 |
Biobank | rs397517918 |
1000 genomes | rs397517918 |
hgdp | rs397517918 |
ensembl | rs397517918 |
geneview | rs397517918 |
scholar | rs397517918 |
rs397517918 | |
pharmgkb | rs397517918 |
gwascentral | rs397517918 |
openSNP | rs397517918 |
23andMe | rs397517918 |
SNPshot | rs397517918 |
SNPdbe | rs397517918 |
MSV3d | rs397517918 |
GWAS Ctlg | rs397517918 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397517918(A;A) |
Alt | rs397517918(A;A) |
Reference | Rs397517918(T;T) |
Significance | Probable-Pathogenic |
Disease | Melnick-Fraser syndrome |
Variation | info |
Gene | EYA1 |
CLNDBN | Melnick-Fraser syndrome |
Reversed | 1 |
HGVS | NC_000008.10:g.72127640A>T |
CLNSRC | ClinVar |
CLNACC | RCV000041389.2, |