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rs3207617

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs3207617(A;T)
Make rs3207617(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position54283899
GeneHNRNPA1
is asnp
is mentioned by
dbSNPrs3207617
ebirs3207617
HLIrs3207617
Exacrs3207617
Varsomers3207617
Maprs3207617
PheGenIrs3207617
hapmaprs3207617
1000 genomesrs3207617
hgdprs3207617
ensemblrs3207617
gopubmedrs3207617
geneviewrs3207617
scholarrs3207617
googlers3207617
pharmgkbrs3207617
gwascentralrs3207617
openSNPrs3207617
23andMers3207617
23andMe allrs3207617
SNP Nexus

SNPshotrs3207617
SNPdbers3207617
MSV3drs3207617
GWAS Ctlgrs3207617
Max Magnitude0
ClinVar
Risk rs3207617(T;T)
Alt rs3207617(T;T)
Reference rs3207617(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,