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rs483353033

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs483353033(A;G)
Make rs483353033(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position54283913
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs483353033
ebirs483353033
HLIrs483353033
Exacrs483353033
Varsomers483353033
Maprs483353033
PheGenIrs483353033
hapmaprs483353033
1000 genomesrs483353033
hgdprs483353033
ensemblrs483353033
gopubmedrs483353033
geneviewrs483353033
scholarrs483353033
googlers483353033
pharmgkbrs483353033
gwascentralrs483353033
openSNPrs483353033
23andMers483353033
23andMe allrs483353033
SNP Nexus

SNPshotrs483353033
SNPdbers483353033
MSV3drs483353033
GWAS Ctlgrs483353033
Max Magnitude0
ClinVar
Risk rs483353033(G;G)
Alt rs483353033(G;G)
Reference rs483353033(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.54677697A>G
CLNSRC
CLNACC RCV000122451.1,