rs727505310
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs727505310(C;T) |
Make rs727505310(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 110812355 |
Gene | RBM20 |
is a | snp |
is | mentioned by |
dbSNP | rs727505310 |
dbSNP (classic) | rs727505310 |
ClinGen | rs727505310 |
ebi | rs727505310 |
HLI | rs727505310 |
Exac | rs727505310 |
Gnomad | rs727505310 |
Varsome | rs727505310 |
LitVar | rs727505310 |
Map | rs727505310 |
PheGenI | rs727505310 |
Biobank | rs727505310 |
1000 genomes | rs727505310 |
hgdp | rs727505310 |
ensembl | rs727505310 |
geneview | rs727505310 |
scholar | rs727505310 |
rs727505310 | |
pharmgkb | rs727505310 |
gwascentral | rs727505310 |
openSNP | rs727505310 |
23andMe | rs727505310 |
SNPshot | rs727505310 |
SNPdbe | rs727505310 |
MSV3d | rs727505310 |
GWAS Ctlg | rs727505310 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs727505310(T;T) |
Alt | rs727505310(T;T) |
Reference | Rs727505310(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | RBM20 |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.112572113C>T |
CLNSRC | |
CLNACC | RCV000156848.2, RCV000183867.1, |