rs747400412
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs747400412(C;T) |
Make rs747400412(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 43943793 |
Gene | LRPPRC |
is a | snp |
is | mentioned by |
dbSNP | rs747400412 |
dbSNP (classic) | rs747400412 |
ClinGen | rs747400412 |
ebi | rs747400412 |
HLI | rs747400412 |
Exac | rs747400412 |
Gnomad | rs747400412 |
Varsome | rs747400412 |
LitVar | rs747400412 |
Map | rs747400412 |
PheGenI | rs747400412 |
Biobank | rs747400412 |
1000 genomes | rs747400412 |
hgdp | rs747400412 |
ensembl | rs747400412 |
geneview | rs747400412 |
scholar | rs747400412 |
rs747400412 | |
pharmgkb | rs747400412 |
gwascentral | rs747400412 |
openSNP | rs747400412 |
23andMe | rs747400412 |
SNPshot | rs747400412 |
SNPdbe | rs747400412 |
MSV3d | rs747400412 |
GWAS Ctlg | rs747400412 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs747400412(T;T) |
Alt | rs747400412(T;T) |
Reference | Rs747400412(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | LRPPRC |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.44170932C>T |
CLNSRC | |
CLNACC | RCV000195452.1, |