rs10876994

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
google	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

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

OMIM	126200
Desc
Variant
Related	also

[PMID 20405052] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.