rs879253855
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs879253855(A;G) |
Make rs879253855(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 123097954 |
Gene | CLMP |
is a | snp |
is | mentioned by |
dbSNP | rs879253855 |
dbSNP (classic) | rs879253855 |
ClinGen | rs879253855 |
ebi | rs879253855 |
HLI | rs879253855 |
Exac | rs879253855 |
Gnomad | rs879253855 |
Varsome | rs879253855 |
LitVar | rs879253855 |
Map | rs879253855 |
PheGenI | rs879253855 |
Biobank | rs879253855 |
1000 genomes | rs879253855 |
hgdp | rs879253855 |
ensembl | rs879253855 |
geneview | rs879253855 |
scholar | rs879253855 |
rs879253855 | |
pharmgkb | rs879253855 |
gwascentral | rs879253855 |
openSNP | rs879253855 |
23andMe | rs879253855 |
SNPshot | rs879253855 |
SNPdbe | rs879253855 |
MSV3d | rs879253855 |
GWAS Ctlg | rs879253855 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879253855(G;G) |
Alt | rs879253855(G;G) |
Reference | Rs879253855(A;A) |
Significance | Pathogenic |
Disease | Congenital short bowel syndrome |
Variation | info |
Gene | CLMP |
CLNDBN | Congenital short bowel syndrome |
Reversed | 1 |
HGVS | NC_000011.9:g.122968662T>C |
CLNSRC | |
CLNACC | RCV000236950.1, |