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rs483353029

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs483353029(C;T)
Make rs483353029(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position54283883
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs483353029
ebirs483353029
HLIrs483353029
Exacrs483353029
Varsomers483353029
Maprs483353029
PheGenIrs483353029
hapmaprs483353029
1000 genomesrs483353029
hgdprs483353029
ensemblrs483353029
gopubmedrs483353029
geneviewrs483353029
scholarrs483353029
googlers483353029
pharmgkbrs483353029
gwascentralrs483353029
openSNPrs483353029
23andMers483353029
23andMe allrs483353029
SNP Nexus

SNPshotrs483353029
SNPdbers483353029
MSV3drs483353029
GWAS Ctlgrs483353029
Max Magnitude0
ClinVar
Risk rs483353029(T;T)
Alt rs483353029(T;T)
Reference rs483353029(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.54677667C>T
CLNSRC
CLNACC RCV000122445.1,