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rs483353024

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs483353024(A;C)
Make rs483353024(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position54283886
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs483353024
ebirs483353024
HLIrs483353024
Exacrs483353024
Varsomers483353024
Maprs483353024
PheGenIrs483353024
hapmaprs483353024
1000 genomesrs483353024
hgdprs483353024
ensemblrs483353024
gopubmedrs483353024
geneviewrs483353024
scholarrs483353024
googlers483353024
pharmgkbrs483353024
gwascentralrs483353024
openSNPrs483353024
23andMers483353024
23andMe allrs483353024
SNP Nexus

SNPshotrs483353024
SNPdbers483353024
MSV3drs483353024
GWAS Ctlgrs483353024
Max Magnitude0
ClinVar
Risk rs483353024(C;C)
Alt rs483353024(C;C)
Reference rs483353024(A;A)
Significance Probable-Pathogenic
Disease Relapsing remitting multiple sclerosis
Variation info
Gene HNRNPA1
CLNDBN Relapsing remitting multiple sclerosis
Reversed 0
HGVS NC_000012.11:g.54677670A>C
CLNSRC
CLNACC RCV000122446.1,