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rs483353030

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs483353030(G;T)
Make rs483353030(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position54283891
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs483353030
ebirs483353030
HLIrs483353030
Exacrs483353030
Varsomers483353030
Maprs483353030
PheGenIrs483353030
hapmaprs483353030
1000 genomesrs483353030
hgdprs483353030
ensemblrs483353030
gopubmedrs483353030
geneviewrs483353030
scholarrs483353030
googlers483353030
pharmgkbrs483353030
gwascentralrs483353030
openSNPrs483353030
23andMers483353030
23andMe allrs483353030
SNP Nexus

SNPshotrs483353030
SNPdbers483353030
MSV3drs483353030
GWAS Ctlgrs483353030
Max Magnitude0
ClinVar
Risk rs483353030(T;T)
Alt rs483353030(T;T)
Reference rs483353030(G;G)
Significance Probable-Pathogenic
Disease Chronic progressive multiple sclerosis
Variation info
Gene HNRNPA1
CLNDBN Chronic progressive multiple sclerosis
Reversed 0
HGVS NC_000012.11:g.54677675G>T
CLNSRC
CLNACC RCV000122447.1,