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rs483353036

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs483353036(C;T)
Make rs483353036(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position54283956
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs483353036
ebirs483353036
HLIrs483353036
Exacrs483353036
Varsomers483353036
Maprs483353036
PheGenIrs483353036
hapmaprs483353036
1000 genomesrs483353036
hgdprs483353036
ensemblrs483353036
gopubmedrs483353036
geneviewrs483353036
scholarrs483353036
googlers483353036
pharmgkbrs483353036
gwascentralrs483353036
openSNPrs483353036
23andMers483353036
23andMe allrs483353036
SNP Nexus

SNPshotrs483353036
SNPdbers483353036
MSV3drs483353036
GWAS Ctlgrs483353036
Max Magnitude0
ClinVar
Risk rs483353036(A,T;A,T)
Alt rs483353036(A,T;A,T)
Reference rs483353036(C;C)
Significance Probable-Pathogenic
Disease Chronic progressive multiple sclerosis
Variation info
Gene HNRNPA1
CLNDBN Chronic progressive multiple sclerosis
Reversed 0
HGVS NC_000012.11:g.54677740C>T
CLNSRC
CLNACC RCV000122454.1,