rs137853155
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs137853155(A;A) |
Make rs137853155(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 10405465 |
Gene | MKKS |
is a | snp |
is | mentioned by |
dbSNP | rs137853155 |
dbSNP (classic) | rs137853155 |
ClinGen | rs137853155 |
ebi | rs137853155 |
HLI | rs137853155 |
Exac | rs137853155 |
Gnomad | rs137853155 |
Varsome | rs137853155 |
LitVar | rs137853155 |
Map | rs137853155 |
PheGenI | rs137853155 |
Biobank | rs137853155 |
1000 genomes | rs137853155 |
hgdp | rs137853155 |
ensembl | rs137853155 |
geneview | rs137853155 |
scholar | rs137853155 |
rs137853155 | |
pharmgkb | rs137853155 |
gwascentral | rs137853155 |
openSNP | rs137853155 |
23andMe | rs137853155 |
SNPshot | rs137853155 |
SNPdbe | rs137853155 |
MSV3d | rs137853155 |
GWAS Ctlg | rs137853155 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137853155(A;A) |
Alt | rs137853155(A;A) |
Reference | Rs137853155(T;T) |
Significance | Untested |
Disease | Bardet-Biedl syndrome 6 |
Variation | info |
Gene | MKKS |
CLNDBN | Bardet-Biedl syndrome 6 |
Reversed | 1 |
HGVS | NC_000020.10:g.10386113A>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | SCV000025826.1, SCV000025826.1, |