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rs483353037

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs483353037(C;T)
Make rs483353037(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position54283958
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs483353037
ebirs483353037
HLIrs483353037
Exacrs483353037
Varsomers483353037
Maprs483353037
PheGenIrs483353037
hapmaprs483353037
1000 genomesrs483353037
hgdprs483353037
ensemblrs483353037
gopubmedrs483353037
geneviewrs483353037
scholarrs483353037
googlers483353037
pharmgkbrs483353037
gwascentralrs483353037
openSNPrs483353037
23andMers483353037
23andMe allrs483353037
SNP Nexus

SNPshotrs483353037
SNPdbers483353037
MSV3drs483353037
GWAS Ctlgrs483353037
Max Magnitude0
ClinVar
Risk rs483353037(T;T)
Alt rs483353037(T;T)
Reference rs483353037(C;C)
Significance Probable-Pathogenic
Disease Chronic progressive multiple sclerosis
Variation info
Gene HNRNPA1
CLNDBN Chronic progressive multiple sclerosis
Reversed 0
HGVS NC_000012.11:g.54677742C>T
CLNSRC
CLNACC RCV000122455.1,