Have questions? Visit https://www.reddit.com/r/SNPedia

rs483353038

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs483353038(A;G)
Make rs483353038(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position54283962
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs483353038
ebirs483353038
HLIrs483353038
Exacrs483353038
Varsomers483353038
Maprs483353038
PheGenIrs483353038
hapmaprs483353038
1000 genomesrs483353038
hgdprs483353038
ensemblrs483353038
gopubmedrs483353038
geneviewrs483353038
scholarrs483353038
googlers483353038
pharmgkbrs483353038
gwascentralrs483353038
openSNPrs483353038
23andMers483353038
23andMe allrs483353038
SNP Nexus

SNPshotrs483353038
SNPdbers483353038
MSV3drs483353038
GWAS Ctlgrs483353038
Max Magnitude0
ClinVar
Risk rs483353038(G;G)
Alt rs483353038(G;G)
Reference rs483353038(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.54677746A>G
CLNSRC
CLNACC RCV000122457.1,