rs483353029

Orientation

plus

Stabilized

plus

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

Make rs483353029(C;T)

Make rs483353029(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

54283883

Gene

HNRNPA1

is a	snp
is	mentioned by
dbSNP	rs483353029
dbSNP (classic)	rs483353029
ClinGen	rs483353029
ebi	rs483353029
HLI	rs483353029
Exac	rs483353029
Gnomad	rs483353029
Varsome	rs483353029
LitVar	rs483353029
Map	rs483353029
PheGenI	rs483353029
Biobank	rs483353029
1000 genomes	rs483353029
hgdp	rs483353029
ensembl	rs483353029
geneview	rs483353029
scholar	rs483353029
google	rs483353029
pharmgkb	rs483353029
gwascentral	rs483353029
openSNP	rs483353029
23andMe	rs483353029
SNPshot	rs483353029
SNPdbe	rs483353029
MSV3d	rs483353029
GWAS Ctlg	rs483353029

Max Magnitude

0

ClinVar
Risk	rs483353029(T;T)
Alt	rs483353029(T;T)
Reference	Rs483353029(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.54677667C>T
CLNSRC
CLNACC	RCV000122445.1,