rs7224488

Orientation

plus

Stabilized

plus

Make rs7224488(A;A)

Make rs7224488(A;C)

Make rs7224488(C;C)

Reference

GRCh38 38.1/142

Chromosome

17

Position

56791264

is a	snp
is	mentioned by
dbSNP	rs7224488
dbSNP (classic)	rs7224488
ClinGen	rs7224488
ebi	rs7224488
HLI	rs7224488
Exac	rs7224488
Gnomad	rs7224488
Varsome	rs7224488
LitVar	rs7224488
Map	rs7224488
PheGenI	rs7224488
Biobank	rs7224488
1000 genomes	rs7224488
hgdp	rs7224488
ensembl	rs7224488
geneview	rs7224488
scholar	rs7224488
google	rs7224488
pharmgkb	rs7224488
gwascentral	rs7224488
openSNP	rs7224488
23andMe	rs7224488
SNPshot	rs7224488
SNPdbe	rs7224488
MSV3d	rs7224488
GWAS Ctlg	rs7224488

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

GWAS snp
PMID	[PMID 24529757]
Trait	Amyotrophic lateral sclerosis (sporadic)
Title	A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
Risk Allele
P-val	2E-6
Odds Ratio	NR NR