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rs1021156

From SNPedia

Orientationminus
Make rs1021156(A;A)
Make rs1021156(A;G)
Make rs1021156(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position78663569
GeneLOC105375911
is asnp
is mentioned by
dbSNPrs1021156
ebirs1021156
HLIrs1021156
Exacrs1021156
Varsomers1021156
Maprs1021156
PheGenIrs1021156
hapmaprs1021156
1000 genomesrs1021156
hgdprs1021156
ensemblrs1021156
gopubmedrs1021156
geneviewrs1021156
scholarrs1021156
googlers1021156
pharmgkbrs1021156
gwascentralrs1021156
openSNPrs1021156
23andMers1021156
23andMe allrs1021156
SNP Nexus

SNPshotrs1021156
SNPdbers1021156
MSV3drs1021156
GWAS Ctlgrs1021156
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 27559181] Role of genetic susceptibility variants in predicting clinical course in multiple sclerosis: a cohort study.