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rs483353032

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs483353032(A;G)
Make rs483353032(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position54283910
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs483353032
ebirs483353032
HLIrs483353032
Exacrs483353032
Varsomers483353032
Maprs483353032
PheGenIrs483353032
hapmaprs483353032
1000 genomesrs483353032
hgdprs483353032
ensemblrs483353032
gopubmedrs483353032
geneviewrs483353032
scholarrs483353032
googlers483353032
pharmgkbrs483353032
gwascentralrs483353032
openSNPrs483353032
23andMers483353032
23andMe allrs483353032
SNP Nexus

SNPshotrs483353032
SNPdbers483353032
MSV3drs483353032
GWAS Ctlgrs483353032
Max Magnitude0
ClinVar
Risk rs483353032(C,G;C,G)
Alt rs483353032(C,G;C,G)
Reference rs483353032(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.54677694A>G
CLNSRC
CLNACC RCV000122450.1,