rs17497526

Orientation

plus

Stabilized

plus

Make rs17497526(C;C)

Make rs17497526(C;T)

Make rs17497526(T;T)

Reference

GRCh38 38.1/142

Chromosome

10

Position

69820364

Gene	COL13A1, LOC105378347

is a	snp
is	mentioned by
dbSNP	rs17497526
dbSNP (classic)	rs17497526
ClinGen	rs17497526
ebi	rs17497526
HLI	rs17497526
Exac	rs17497526
Gnomad	rs17497526
Varsome	rs17497526
LitVar	rs17497526
Map	rs17497526
PheGenI	rs17497526
Biobank	rs17497526
1000 genomes	rs17497526
hgdp	rs17497526
ensembl	rs17497526
geneview	rs17497526
scholar	rs17497526
google	rs17497526
pharmgkb	rs17497526
gwascentral	rs17497526
openSNP	rs17497526
23andMe	rs17497526
SNPshot	rs17497526
SNPdbe	rs17497526
MSV3d	rs17497526
GWAS Ctlg	rs17497526

GMAF

0.06933

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 23793441]
Trait	Parkinson's disease
Title	Parkinson disease loci in the mid-western Amish.
Risk Allele	G
P-val	6E-7
Odds Ratio	NR NR