rs10896380
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs10896380(A;G) |
Make rs10896380(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 68914934 |
Gene | IGHMBP2 |
is a | snp |
is | mentioned by |
dbSNP | rs10896380 |
dbSNP (classic) | rs10896380 |
ClinGen | rs10896380 |
ebi | rs10896380 |
HLI | rs10896380 |
Exac | rs10896380 |
Gnomad | rs10896380 |
Varsome | rs10896380 |
LitVar | rs10896380 |
Map | rs10896380 |
PheGenI | rs10896380 |
Biobank | rs10896380 |
1000 genomes | rs10896380 |
hgdp | rs10896380 |
ensembl | rs10896380 |
geneview | rs10896380 |
scholar | rs10896380 |
rs10896380 | |
pharmgkb | rs10896380 |
gwascentral | rs10896380 |
openSNP | rs10896380 |
23andMe | rs10896380 |
SNPshot | rs10896380 |
SNPdbe | rs10896380 |
MSV3d | rs10896380 |
GWAS Ctlg | rs10896380 |
GMAF | 0.157 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs10896380(G;G) |
Alt | rs10896380(G;G) |
Reference | Rs10896380(A;A) |
Significance | Non-pathogenic |
Disease | not specified Spinal muscular atrophy |
Variation | info |
Gene | IGHMBP2 |
CLNDBN | not specified Spinal muscular atrophy |
Reversed | 0 |
HGVS | NC_000011.9:g.68682402A>G |
CLNSRC | |
CLNACC | RCV000244835.1, RCV000388182.1, |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 11
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Affy500k
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d