rs200686732
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs200686732(C;T) |
Make rs200686732(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 43995941 |
Gene | LRPPRC |
is a | snp |
is | mentioned by |
dbSNP | rs200686732 |
dbSNP (classic) | rs200686732 |
ClinGen | rs200686732 |
ebi | rs200686732 |
HLI | rs200686732 |
Exac | rs200686732 |
Gnomad | rs200686732 |
Varsome | rs200686732 |
LitVar | rs200686732 |
Map | rs200686732 |
PheGenI | rs200686732 |
Biobank | rs200686732 |
1000 genomes | rs200686732 |
hgdp | rs200686732 |
ensembl | rs200686732 |
geneview | rs200686732 |
scholar | rs200686732 |
rs200686732 | |
pharmgkb | rs200686732 |
gwascentral | rs200686732 |
openSNP | rs200686732 |
23andMe | rs200686732 |
SNPshot | rs200686732 |
SNPdbe | rs200686732 |
MSV3d | rs200686732 |
GWAS Ctlg | rs200686732 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs200686732(A;A) rs200686732(G;G) rs200686732(T;T) |
Alt | rs200686732(A;A) rs200686732(G;G) rs200686732(T;T) |
Reference | Rs200686732(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | LRPPRC |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.44223080C>T |
CLNSRC | |
CLNACC | RCV000199897.1, |