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rs6871748

From SNPedia

Orientationplus
Stabilizedplus
Make rs6871748(C;C)
Make rs6871748(C;T)
Make rs6871748(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position35885880
is asnp
is mentioned by
dbSNPrs6871748
ebirs6871748
HLIrs6871748
Exacrs6871748
Varsomers6871748
Maprs6871748
PheGenIrs6871748
hapmaprs6871748
1000 genomesrs6871748
hgdprs6871748
ensemblrs6871748
gopubmedrs6871748
geneviewrs6871748
scholarrs6871748
googlers6871748
pharmgkbrs6871748
gwascentralrs6871748
openSNPrs6871748
23andMers6871748
23andMe allrs6871748
SNP Nexus

SNPshotrs6871748
SNPdbers6871748
MSV3drs6871748
GWAS Ctlgrs6871748
GMAF0.1938
Max Magnitude
? (C;C) (C;T) (T;T) 28
OMIM612595
DescMULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 3; MS3
Variant
Relatedalso
[PMID 19221116OA-icon.png] Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.


GET Evidence
rs6871748
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.18254
summary