rs10145110

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common genotype

Make rs10145110(C;T)

Make rs10145110(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

101008533

is a	snp
is	mentioned by
dbSNP	rs10145110
dbSNP (classic)	rs10145110
ClinGen	rs10145110
ebi	rs10145110
HLI	rs10145110
Exac	rs10145110
Gnomad	rs10145110
Varsome	rs10145110
LitVar	rs10145110
Map	rs10145110
PheGenI	rs10145110
Biobank	rs10145110
1000 genomes	rs10145110
hgdp	rs10145110
ensembl	rs10145110
geneview	rs10145110
scholar	rs10145110
google	rs10145110
pharmgkb	rs10145110
gwascentral	rs10145110
openSNP	rs10145110
23andMe	rs10145110
SNPshot	rs10145110
SNPdbe	rs10145110
MSV3d	rs10145110
GWAS Ctlg	rs10145110

Max Magnitude

0

?	(C;C) (C;T) (T;T)	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	1E-7
Odds Ratio	NR NR