rs483353025

Orientation

plus

Stabilized

plus

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

Make rs483353025(A;G)

Make rs483353025(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

54283899

Gene

HNRNPA1

is a	snp
is	mentioned by
dbSNP	rs483353025
dbSNP (classic)	rs483353025
ClinGen	rs483353025
ebi	rs483353025
HLI	rs483353025
Exac	rs483353025
Gnomad	rs483353025
Varsome	rs483353025
LitVar	rs483353025
Map	rs483353025
PheGenI	rs483353025
Biobank	rs483353025
1000 genomes	rs483353025
hgdp	rs483353025
ensembl	rs483353025
geneview	rs483353025
scholar	rs483353025
google	rs483353025
pharmgkb	rs483353025
gwascentral	rs483353025
openSNP	rs483353025
23andMe	rs483353025
SNPshot	rs483353025
SNPdbe	rs483353025
MSV3d	rs483353025
GWAS Ctlg	rs483353025

Max Magnitude

0

ClinVar
Risk	rs483353025(G;G)
Alt	rs483353025(G;G)
Reference	Rs483353025(A;A)
Significance	Probable-Pathogenic
Disease	Relapsing remitting multiple sclerosis
Variation	info
Gene	HNRNPA1
CLNDBN	Relapsing remitting multiple sclerosis
Reversed	0
HGVS	NC_000012.11:g.54677683A>G
CLNSRC
CLNACC	RCV000122448.1,