rs765911841
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs765911841(C;C) |
Make rs765911841(C;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 43976185 |
Gene | LRPPRC |
is a | snp |
is | mentioned by |
dbSNP | rs765911841 |
dbSNP (classic) | rs765911841 |
ClinGen | rs765911841 |
ebi | rs765911841 |
HLI | rs765911841 |
Exac | rs765911841 |
Gnomad | rs765911841 |
Varsome | rs765911841 |
LitVar | rs765911841 |
Map | rs765911841 |
PheGenI | rs765911841 |
Biobank | rs765911841 |
1000 genomes | rs765911841 |
hgdp | rs765911841 |
ensembl | rs765911841 |
geneview | rs765911841 |
scholar | rs765911841 |
rs765911841 | |
pharmgkb | rs765911841 |
gwascentral | rs765911841 |
openSNP | rs765911841 |
23andMe | rs765911841 |
SNPshot | rs765911841 |
SNPdbe | rs765911841 |
MSV3d | rs765911841 |
GWAS Ctlg | rs765911841 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs765911841(C;C) |
Alt | rs765911841(C;C) |
Reference | Rs765911841(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | LRPPRC |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.44203324T>C |
CLNSRC | |
CLNACC | RCV000200430.1, |