rs113994196
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs113994196(-;CCTG) |
Make rs113994196(CCTG;CCTG) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 10412638 |
Gene | MKKS |
is a | snp |
is | mentioned by |
dbSNP | rs113994196 |
dbSNP (classic) | rs113994196 |
ClinGen | rs113994196 |
ebi | rs113994196 |
HLI | rs113994196 |
Exac | rs113994196 |
Gnomad | rs113994196 |
Varsome | rs113994196 |
LitVar | rs113994196 |
Map | rs113994196 |
PheGenI | rs113994196 |
Biobank | rs113994196 |
1000 genomes | rs113994196 |
hgdp | rs113994196 |
ensembl | rs113994196 |
geneview | rs113994196 |
scholar | rs113994196 |
rs113994196 | |
pharmgkb | rs113994196 |
gwascentral | rs113994196 |
openSNP | rs113994196 |
23andMe | rs113994196 |
SNPshot | rs113994196 |
SNPdbe | rs113994196 |
MSV3d | rs113994196 |
GWAS Ctlg | rs113994196 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs113994196(CCTG;CCTG) |
Alt | rs113994196(CCTG;CCTG) |
Reference | Rs113994196(-;-) |
Significance | Pathogenic |
Disease | Bardet-Biedl syndrome |
Variation | info |
Gene | MKKS |
CLNDBN | Bardet-Biedl syndrome |
Reversed | 1 |
HGVS | NC_000020.10:g.10393286_10393287insCAGG |
CLNSRC | ClinVar GeneReviews |
CLNACC | RCV000020862.1, |
[PMID 12107442] Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patients.