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rs483353039

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs483353039(A;G)
Make rs483353039(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position54283961
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs483353039
ebirs483353039
HLIrs483353039
Exacrs483353039
Varsomers483353039
Maprs483353039
PheGenIrs483353039
hapmaprs483353039
1000 genomesrs483353039
hgdprs483353039
ensemblrs483353039
gopubmedrs483353039
geneviewrs483353039
scholarrs483353039
googlers483353039
pharmgkbrs483353039
gwascentralrs483353039
openSNPrs483353039
23andMers483353039
23andMe allrs483353039
SNP Nexus

SNPshotrs483353039
SNPdbers483353039
MSV3drs483353039
GWAS Ctlgrs483353039
Max Magnitude0
ClinVar
Risk rs483353039(G;G)
Alt rs483353039(G;G)
Reference rs483353039(A;A)
Significance Probable-Pathogenic
Disease Chronic progressive multiple sclerosis
Variation info
Gene HNRNPA1
CLNDBN Chronic progressive multiple sclerosis
Reversed 0
HGVS NC_000012.11:g.54677745A>G
CLNSRC
CLNACC RCV000122456.1,