rs1035033641
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 6615257 |
Gene | TPP1 |
is a | snp |
is | mentioned by |
dbSNP | rs1035033641 |
dbSNP (classic) | rs1035033641 |
ClinGen | rs1035033641 |
ebi | rs1035033641 |
HLI | rs1035033641 |
Exac | rs1035033641 |
Gnomad | rs1035033641 |
Varsome | rs1035033641 |
LitVar | rs1035033641 |
Map | rs1035033641 |
PheGenI | rs1035033641 |
Biobank | rs1035033641 |
1000 genomes | rs1035033641 |
hgdp | rs1035033641 |
ensembl | rs1035033641 |
geneview | rs1035033641 |
scholar | rs1035033641 |
rs1035033641 | |
pharmgkb | rs1035033641 |
gwascentral | rs1035033641 |
openSNP | rs1035033641 |
23andMe | rs1035033641 |
SNPshot | rs1035033641 |
SNPdbe | rs1035033641 |
MSV3d | rs1035033641 |
GWAS Ctlg | rs1035033641 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1035033641(A;A) |
Alt | rs1035033641(A;A) |
Reference | Rs1035033641(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.6636488G>A |
CLNSRC | |
CLNACC | RCV000489192.1, |