rs149969786
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs149969786(A;G) |
Make rs149969786(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 15 |
Position | 42410949 |
Gene | CAPN3 |
is a | snp |
is | mentioned by |
dbSNP | rs149969786 |
dbSNP (classic) | rs149969786 |
ClinGen | rs149969786 |
ebi | rs149969786 |
HLI | rs149969786 |
Exac | rs149969786 |
Gnomad | rs149969786 |
Varsome | rs149969786 |
LitVar | rs149969786 |
Map | rs149969786 |
PheGenI | rs149969786 |
Biobank | rs149969786 |
1000 genomes | rs149969786 |
hgdp | rs149969786 |
ensembl | rs149969786 |
geneview | rs149969786 |
scholar | rs149969786 |
rs149969786 | |
pharmgkb | rs149969786 |
gwascentral | rs149969786 |
openSNP | rs149969786 |
23andMe | rs149969786 |
SNPshot | rs149969786 |
SNPdbe | rs149969786 |
MSV3d | rs149969786 |
GWAS Ctlg | rs149969786 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs149969786(G;G) |
Alt | rs149969786(G;G) |
Reference | Rs149969786(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CAPN3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.42703147A>G |
CLNSRC | |
CLNACC | RCV000171232.1, |