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rs483353035

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs483353035(C;C)
Make rs483353035(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position54283946
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs483353035
ebirs483353035
HLIrs483353035
Exacrs483353035
Varsomers483353035
Maprs483353035
PheGenIrs483353035
hapmaprs483353035
1000 genomesrs483353035
hgdprs483353035
ensemblrs483353035
gopubmedrs483353035
geneviewrs483353035
scholarrs483353035
googlers483353035
pharmgkbrs483353035
gwascentralrs483353035
openSNPrs483353035
23andMers483353035
23andMe allrs483353035
SNP Nexus

SNPshotrs483353035
SNPdbers483353035
MSV3drs483353035
GWAS Ctlgrs483353035
Max Magnitude0
ClinVar
Risk rs483353035(C;C)
Alt rs483353035(C;C)
Reference rs483353035(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.54677730T>C
CLNSRC
CLNACC RCV000122453.1,