rs10876994
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10876994(A;A) |
Make rs10876994(A;C) |
Make rs10876994(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 57670954 |
is a | snp |
is | mentioned by |
dbSNP | rs10876994 |
dbSNP (classic) | rs10876994 |
ClinGen | rs10876994 |
ebi | rs10876994 |
HLI | rs10876994 |
Exac | rs10876994 |
Gnomad | rs10876994 |
Varsome | rs10876994 |
LitVar | rs10876994 |
Map | rs10876994 |
PheGenI | rs10876994 |
Biobank | rs10876994 |
1000 genomes | rs10876994 |
hgdp | rs10876994 |
ensembl | rs10876994 |
geneview | rs10876994 |
scholar | rs10876994 |
rs10876994 | |
pharmgkb | rs10876994 |
gwascentral | rs10876994 |
openSNP | rs10876994 |
23andMe | rs10876994 |
SNPshot | rs10876994 |
SNPdbe | rs10876994 |
MSV3d | rs10876994 |
GWAS Ctlg | rs10876994 |
GMAF | 0.3049 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
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[PMID 19525955] Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
[PMID 20405052] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.