rs114970039
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs114970039(C;C) |
Make rs114970039(C;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 198754304 |
Gene | PTPRC |
is a | snp |
is | mentioned by |
dbSNP | rs114970039 |
dbSNP (classic) | rs114970039 |
ClinGen | rs114970039 |
ebi | rs114970039 |
HLI | rs114970039 |
Exac | rs114970039 |
Gnomad | rs114970039 |
Varsome | rs114970039 |
LitVar | rs114970039 |
Map | rs114970039 |
PheGenI | rs114970039 |
Biobank | rs114970039 |
1000 genomes | rs114970039 |
hgdp | rs114970039 |
ensembl | rs114970039 |
geneview | rs114970039 |
scholar | rs114970039 |
rs114970039 | |
pharmgkb | rs114970039 |
gwascentral | rs114970039 |
openSNP | rs114970039 |
23andMe | rs114970039 |
SNPshot | rs114970039 |
SNPdbe | rs114970039 |
MSV3d | rs114970039 |
GWAS Ctlg | rs114970039 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs114970039(C;C) |
Alt | rs114970039(C;C) |
Reference | Rs114970039(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PTPRC |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.198723433T>C |
CLNSRC | |
CLNACC | RCV000171165.1, |