rs483353033

Orientation

plus

Stabilized

plus

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

Make rs483353033(A;G)

Make rs483353033(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

54283913

Gene

HNRNPA1

is a	snp
is	mentioned by
dbSNP	rs483353033
dbSNP (classic)	rs483353033
ClinGen	rs483353033
ebi	rs483353033
HLI	rs483353033
Exac	rs483353033
Gnomad	rs483353033
Varsome	rs483353033
LitVar	rs483353033
Map	rs483353033
PheGenI	rs483353033
Biobank	rs483353033
1000 genomes	rs483353033
hgdp	rs483353033
ensembl	rs483353033
geneview	rs483353033
scholar	rs483353033
google	rs483353033
pharmgkb	rs483353033
gwascentral	rs483353033
openSNP	rs483353033
23andMe	rs483353033
SNPshot	rs483353033
SNPdbe	rs483353033
MSV3d	rs483353033
GWAS Ctlg	rs483353033

Max Magnitude

0

ClinVar
Risk	rs483353033(G;G)
Alt	rs483353033(G;G)
Reference	Rs483353033(A;A)
Significance	Probable-Pathogenic
Disease	Chronic progressive multiple sclerosis
Variation	info
Gene	HNRNPA1
CLNDBN	Chronic progressive multiple sclerosis
Reversed	0
HGVS	NC_000012.11:g.54677697A>G
CLNSRC
CLNACC	RCV000122451.1,