rs121917767

Orientation

plus

Stabilized

plus

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

Make rs121917767(C;G)

Make rs121917767(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

41260751

Gene

UCHL1

is a	snp
is	mentioned by
dbSNP	rs121917767
dbSNP (classic)	rs121917767
ClinGen	rs121917767
ebi	rs121917767
HLI	rs121917767
Exac	rs121917767
Gnomad	rs121917767
Varsome	rs121917767
LitVar	rs121917767
Map	rs121917767
PheGenI	rs121917767
Biobank	rs121917767
1000 genomes	rs121917767
hgdp	rs121917767
ensembl	rs121917767
geneview	rs121917767
scholar	rs121917767
google	rs121917767
pharmgkb	rs121917767
gwascentral	rs121917767
openSNP	rs121917767
23andMe	rs121917767
SNPshot	rs121917767
SNPdbe	rs121917767
MSV3d	rs121917767
GWAS Ctlg	rs121917767

Max Magnitude

0

OMIM	191342
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121917767(G;G) rs121917767(T;T)
Alt	rs121917767(G;G) rs121917767(T;T)
Reference	Rs121917767(C;C)
Significance	Other
Disease	Parkinson disease 5
Variation	info
Gene	UCHL1
CLNDBN	Parkinson disease 5
Reversed	0
HGVS	NC_000004.11:g.41262768C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013091.28,