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rs483353025

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs483353025(A;G)
Make rs483353025(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position54283899
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs483353025
ebirs483353025
HLIrs483353025
Exacrs483353025
Varsomers483353025
Maprs483353025
PheGenIrs483353025
hapmaprs483353025
1000 genomesrs483353025
hgdprs483353025
ensemblrs483353025
gopubmedrs483353025
geneviewrs483353025
scholarrs483353025
googlers483353025
pharmgkbrs483353025
gwascentralrs483353025
openSNPrs483353025
23andMers483353025
23andMe allrs483353025
SNP Nexus

SNPshotrs483353025
SNPdbers483353025
MSV3drs483353025
GWAS Ctlgrs483353025
Max Magnitude0
ClinVar
Risk rs483353025(G;G)
Alt rs483353025(G;G)
Reference rs483353025(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.54677683A>G
CLNSRC
CLNACC RCV000122448.1,