rs201060167
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs201060167(C;C) |
Make rs201060167(C;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 68929204 |
Gene | IGHMBP2 |
is a | snp |
is | mentioned by |
dbSNP | rs201060167 |
dbSNP (classic) | rs201060167 |
ClinGen | rs201060167 |
ebi | rs201060167 |
HLI | rs201060167 |
Exac | rs201060167 |
Gnomad | rs201060167 |
Varsome | rs201060167 |
LitVar | rs201060167 |
Map | rs201060167 |
PheGenI | rs201060167 |
Biobank | rs201060167 |
1000 genomes | rs201060167 |
hgdp | rs201060167 |
ensembl | rs201060167 |
geneview | rs201060167 |
scholar | rs201060167 |
rs201060167 | |
pharmgkb | rs201060167 |
gwascentral | rs201060167 |
openSNP | rs201060167 |
23andMe | rs201060167 |
SNPshot | rs201060167 |
SNPdbe | rs201060167 |
MSV3d | rs201060167 |
GWAS Ctlg | rs201060167 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201060167(C;C) |
Alt | rs201060167(C;C) |
Reference | Rs201060167(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | IGHMBP2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.68696672T>C |
CLNSRC | |
CLNACC | RCV000236185.2, |