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rs483353022

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs483353022(C;C)
Make rs483353022(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position54283847
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs483353022
ebirs483353022
HLIrs483353022
Exacrs483353022
Varsomers483353022
Maprs483353022
PheGenIrs483353022
hapmaprs483353022
1000 genomesrs483353022
hgdprs483353022
ensemblrs483353022
gopubmedrs483353022
geneviewrs483353022
scholarrs483353022
googlers483353022
pharmgkbrs483353022
gwascentralrs483353022
openSNPrs483353022
23andMers483353022
23andMe allrs483353022
SNP Nexus

SNPshotrs483353022
SNPdbers483353022
MSV3drs483353022
GWAS Ctlgrs483353022
Max Magnitude0
ClinVar
Risk rs483353022(C;C)
Alt rs483353022(C;C)
Reference rs483353022(T;T)
Significance Probable-Pathogenic
Disease Chronic progressive multiple sclerosis
Variation info
Gene HNRNPA1
CLNDBN Chronic progressive multiple sclerosis
Reversed 0
HGVS NC_000012.11:g.54677631T>C
CLNSRC
CLNACC RCV000122441.1,