rs483353022

Orientation

plus

Stabilized

plus

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

Make rs483353022(C;C)

Make rs483353022(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

54283847

Gene

HNRNPA1

is a	snp
is	mentioned by
dbSNP	rs483353022
dbSNP (classic)	rs483353022
ClinGen	rs483353022
ebi	rs483353022
HLI	rs483353022
Exac	rs483353022
Gnomad	rs483353022
Varsome	rs483353022
LitVar	rs483353022
Map	rs483353022
PheGenI	rs483353022
Biobank	rs483353022
1000 genomes	rs483353022
hgdp	rs483353022
ensembl	rs483353022
geneview	rs483353022
scholar	rs483353022
google	rs483353022
pharmgkb	rs483353022
gwascentral	rs483353022
openSNP	rs483353022
23andMe	rs483353022
SNPshot	rs483353022
SNPdbe	rs483353022
MSV3d	rs483353022
GWAS Ctlg	rs483353022

Max Magnitude

0

ClinVar
Risk	rs483353022(C;C)
Alt	rs483353022(C;C)
Reference	Rs483353022(T;T)
Significance	Probable-Pathogenic
Disease	Chronic progressive multiple sclerosis
Variation	info
Gene	HNRNPA1
CLNDBN	Chronic progressive multiple sclerosis
Reversed	0
HGVS	NC_000012.11:g.54677631T>C
CLNSRC
CLNACC	RCV000122441.1,