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rs483353034

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs483353034(A;G)
Make rs483353034(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position54283944
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs483353034
ebirs483353034
HLIrs483353034
Exacrs483353034
Varsomers483353034
Maprs483353034
PheGenIrs483353034
hapmaprs483353034
1000 genomesrs483353034
hgdprs483353034
ensemblrs483353034
gopubmedrs483353034
geneviewrs483353034
scholarrs483353034
googlers483353034
pharmgkbrs483353034
gwascentralrs483353034
openSNPrs483353034
23andMers483353034
23andMe allrs483353034
SNP Nexus

SNPshotrs483353034
SNPdbers483353034
MSV3drs483353034
GWAS Ctlgrs483353034
Max Magnitude0
ClinVar
Risk rs483353034(G;G)
Alt rs483353034(G;G)
Reference rs483353034(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.54677728A>G
CLNSRC
CLNACC RCV000122452.1,