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rs2303137

From SNPedia

Orientationminus
Stabilizedminus
Make rs2303137(A;A)
Make rs2303137(A;T)
Make rs2303137(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position35895623
is asnp
is mentioned by
dbSNPrs2303137
ebirs2303137
HLIrs2303137
Exacrs2303137
Varsomers2303137
Maprs2303137
PheGenIrs2303137
hapmaprs2303137
1000 genomesrs2303137
hgdprs2303137
ensemblrs2303137
gopubmedrs2303137
geneviewrs2303137
scholarrs2303137
googlers2303137
pharmgkbrs2303137
gwascentralrs2303137
openSNPrs2303137
23andMers2303137
23andMe allrs2303137
SNP Nexus

SNPshotrs2303137
SNPdbers2303137
MSV3drs2303137
GWAS Ctlgrs2303137
GMAF0.4812
Max Magnitude
? (A;A) (A;T) (T;T) 28
OMIM612595
DescMULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 3; MS3
Variant
Relatedalso



GET Evidence
rs2303137
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.414062
summary