rs483353035

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs483353035(C;C)

Make rs483353035(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

54283946

Gene

HNRNPA1

is a	snp
is	mentioned by
dbSNP	rs483353035
dbSNP (classic)	rs483353035
ClinGen	rs483353035
ebi	rs483353035
HLI	rs483353035
Exac	rs483353035
Gnomad	rs483353035
Varsome	rs483353035
LitVar	rs483353035
Map	rs483353035
PheGenI	rs483353035
Biobank	rs483353035
1000 genomes	rs483353035
hgdp	rs483353035
ensembl	rs483353035
geneview	rs483353035
scholar	rs483353035
google	rs483353035
pharmgkb	rs483353035
gwascentral	rs483353035
openSNP	rs483353035
23andMe	rs483353035
SNPshot	rs483353035
SNPdbe	rs483353035
MSV3d	rs483353035
GWAS Ctlg	rs483353035

Max Magnitude

0

ClinVar
Risk	rs483353035(C;C)
Alt	rs483353035(C;C)
Reference	Rs483353035(T;T)
Significance	Probable-Pathogenic
Disease	Chronic progressive multiple sclerosis
Variation	info
Gene	HNRNPA1
CLNDBN	Chronic progressive multiple sclerosis
Reversed	0
HGVS	NC_000012.11:g.54677730T>C
CLNSRC
CLNACC	RCV000122453.1,