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rs483353031

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs483353031(C;C)
Make rs483353031(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position54283901
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs483353031
ebirs483353031
HLIrs483353031
Exacrs483353031
Varsomers483353031
Maprs483353031
PheGenIrs483353031
hapmaprs483353031
1000 genomesrs483353031
hgdprs483353031
ensemblrs483353031
gopubmedrs483353031
geneviewrs483353031
scholarrs483353031
googlers483353031
pharmgkbrs483353031
gwascentralrs483353031
openSNPrs483353031
23andMers483353031
23andMe allrs483353031
SNP Nexus

SNPshotrs483353031
SNPdbers483353031
MSV3drs483353031
GWAS Ctlgrs483353031
Max Magnitude0
ClinVar
Risk rs483353031(C;C)
Alt rs483353031(C;C)
Reference rs483353031(T;T)
Significance Pathogenic
Disease Chronic progressive multiple sclerosis
Variation info
Gene HNRNPA1
CLNDBN Chronic progressive multiple sclerosis
Reversed 0
HGVS NC_000012.11:g.54677685T>C
CLNSRC
CLNACC RCV000122449.1,