rs483353037

Orientation

plus

Stabilized

plus

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

Make rs483353037(C;T)

Make rs483353037(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

54283958

Gene

HNRNPA1

is a	snp
is	mentioned by
dbSNP	rs483353037
dbSNP (classic)	rs483353037
ClinGen	rs483353037
ebi	rs483353037
HLI	rs483353037
Exac	rs483353037
Gnomad	rs483353037
Varsome	rs483353037
LitVar	rs483353037
Map	rs483353037
PheGenI	rs483353037
Biobank	rs483353037
1000 genomes	rs483353037
hgdp	rs483353037
ensembl	rs483353037
geneview	rs483353037
scholar	rs483353037
google	rs483353037
pharmgkb	rs483353037
gwascentral	rs483353037
openSNP	rs483353037
23andMe	rs483353037
SNPshot	rs483353037
SNPdbe	rs483353037
MSV3d	rs483353037
GWAS Ctlg	rs483353037

Max Magnitude

0

ClinVar
Risk	rs483353037(T;T)
Alt	rs483353037(T;T)
Reference	Rs483353037(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.54677742C>T
CLNSRC
CLNACC	RCV000122455.1,