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rs10876994

From SNPedia

Orientationplus
Stabilizedplus
Make rs10876994(A;A)
Make rs10876994(A;C)
Make rs10876994(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position57670954
is asnp
is mentioned by
dbSNPrs10876994
ebirs10876994
HLIrs10876994
Exacrs10876994
Varsomers10876994
Maprs10876994
PheGenIrs10876994
hapmaprs10876994
1000 genomesrs10876994
hgdprs10876994
ensemblrs10876994
gopubmedrs10876994
geneviewrs10876994
scholarrs10876994
googlers10876994
pharmgkbrs10876994
gwascentralrs10876994
openSNPrs10876994
23andMers10876994
23andMe allrs10876994
SNP Nexus

SNPshotrs10876994
SNPdbers10876994
MSV3drs10876994
GWAS Ctlgrs10876994
GMAF0.3049
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 19525955] Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20

OMIM126200
Desc
Variant
Relatedalso
[PMID 20405052OA-icon.png] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.