rs587777841
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587777841(C;G) |
Make rs587777841(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 13 |
Position | 27623011 |
Gene | LNX2, POLR1D |
is a | snp |
is | mentioned by |
dbSNP | rs587777841 |
dbSNP (classic) | rs587777841 |
ClinGen | rs587777841 |
ebi | rs587777841 |
HLI | rs587777841 |
Exac | rs587777841 |
Gnomad | rs587777841 |
Varsome | rs587777841 |
LitVar | rs587777841 |
Map | rs587777841 |
PheGenI | rs587777841 |
Biobank | rs587777841 |
1000 genomes | rs587777841 |
hgdp | rs587777841 |
ensembl | rs587777841 |
geneview | rs587777841 |
scholar | rs587777841 |
rs587777841 | |
pharmgkb | rs587777841 |
gwascentral | rs587777841 |
openSNP | rs587777841 |
23andMe | rs587777841 |
SNPshot | rs587777841 |
SNPdbe | rs587777841 |
MSV3d | rs587777841 |
GWAS Ctlg | rs587777841 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587777841(G;G) |
Alt | rs587777841(G;G) |
Reference | Rs587777841(C;C) |
Significance | Pathogenic |
Disease | Treacher Collins syndrome 2 |
Variation | info |
Gene | POLR1D |
CLNDBN | Treacher Collins syndrome 2 |
Reversed | 0 |
HGVS | NC_000013.10:g.28197148C>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000144520.3, |