rs483353031

Orientation

plus

Stabilized

plus

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

Make rs483353031(C;C)

Make rs483353031(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

54283901

Gene

HNRNPA1

is a	snp
is	mentioned by
dbSNP	rs483353031
dbSNP (classic)	rs483353031
ClinGen	rs483353031
ebi	rs483353031
HLI	rs483353031
Exac	rs483353031
Gnomad	rs483353031
Varsome	rs483353031
LitVar	rs483353031
Map	rs483353031
PheGenI	rs483353031
Biobank	rs483353031
1000 genomes	rs483353031
hgdp	rs483353031
ensembl	rs483353031
geneview	rs483353031
scholar	rs483353031
google	rs483353031
pharmgkb	rs483353031
gwascentral	rs483353031
openSNP	rs483353031
23andMe	rs483353031
SNPshot	rs483353031
SNPdbe	rs483353031
MSV3d	rs483353031
GWAS Ctlg	rs483353031

Max Magnitude

0

ClinVar
Risk	rs483353031(C;C)
Alt	rs483353031(C;C)
Reference	Rs483353031(T;T)
Significance	Pathogenic
Disease	Chronic progressive multiple sclerosis
Variation	info
Gene	HNRNPA1
CLNDBN	Chronic progressive multiple sclerosis
Reversed	0
HGVS	NC_000012.11:g.54677685T>C
CLNSRC
CLNACC	RCV000122449.1,