rs121908162
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121908162(C;T) |
Make rs121908162(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 10324838 |
Gene | KIF1B |
is a | snp |
is | mentioned by |
dbSNP | rs121908162 |
dbSNP (classic) | rs121908162 |
ClinGen | rs121908162 |
ebi | rs121908162 |
HLI | rs121908162 |
Exac | rs121908162 |
Gnomad | rs121908162 |
Varsome | rs121908162 |
LitVar | rs121908162 |
Map | rs121908162 |
PheGenI | rs121908162 |
Biobank | rs121908162 |
1000 genomes | rs121908162 |
hgdp | rs121908162 |
ensembl | rs121908162 |
geneview | rs121908162 |
scholar | rs121908162 |
rs121908162 | |
pharmgkb | rs121908162 |
gwascentral | rs121908162 |
openSNP | rs121908162 |
23andMe | rs121908162 |
SNPshot | rs121908162 |
SNPdbe | rs121908162 |
MSV3d | rs121908162 |
GWAS Ctlg | rs121908162 |
GMAF | 0.0009183 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121908162(T;T) |
Alt | rs121908162(T;T) |
Reference | Rs121908162(C;C) |
Significance | Other |
Disease | Neuroblastoma 1 Charcot-Marie-Tooth disease |
Variation | info |
Gene | KIF1B |
CLNDBN | Neuroblastoma 1 Charcot-Marie-Tooth disease, type 2 |
Reversed | 0 |
HGVS | NC_000001.10:g.10384896C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000004923.2, RCV000198737.2, |