rs587776862
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GCCTGAGGAGGA;GCCTGAGGAGGA) | 0 | common in clinvar |
Make rs587776862(GCCTGAGGAGGA;T) |
Make rs587776862(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 239908624 |
Gene | CHRM3 |
is a | snp |
is | mentioned by |
dbSNP | rs587776862 |
dbSNP (classic) | rs587776862 |
ClinGen | rs587776862 |
ebi | rs587776862 |
HLI | rs587776862 |
Exac | rs587776862 |
Gnomad | rs587776862 |
Varsome | rs587776862 |
LitVar | rs587776862 |
Map | rs587776862 |
PheGenI | rs587776862 |
Biobank | rs587776862 |
1000 genomes | rs587776862 |
hgdp | rs587776862 |
ensembl | rs587776862 |
geneview | rs587776862 |
scholar | rs587776862 |
rs587776862 | |
pharmgkb | rs587776862 |
gwascentral | rs587776862 |
openSNP | rs587776862 |
23andMe | rs587776862 |
SNPshot | rs587776862 |
SNPdbe | rs587776862 |
MSV3d | rs587776862 |
GWAS Ctlg | rs587776862 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587776862(T;T) |
Alt | rs587776862(T;T) |
Reference | Rs587776862(GCCTGAGGAGGA;GCCTGAGGAGGA) |
Significance | Pathogenic |
Disease | Prune belly syndrome |
Variation | info |
Gene | CHRM3 |
CLNDBN | Prune belly syndrome |
Reversed | 0 |
HGVS | NC_000001.10:g.240071924_240071935delGCCTGAGGAGGAinsT |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000022466.30, |