rs201106962

Orientation

plus

Stabilized

plus

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

Make rs201106962(A;C)

Make rs201106962(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

89828156

Gene

SNCA

is a	snp
is	mentioned by
dbSNP	rs201106962
dbSNP (classic)	rs201106962
ClinGen	rs201106962
ebi	rs201106962
HLI	rs201106962
Exac	rs201106962
Gnomad	rs201106962
Varsome	rs201106962
LitVar	rs201106962
Map	rs201106962
PheGenI	rs201106962
Biobank	rs201106962
1000 genomes	rs201106962
hgdp	rs201106962
ensembl	rs201106962
geneview	rs201106962
scholar	rs201106962
google	rs201106962
pharmgkb	rs201106962
gwascentral	rs201106962
openSNP	rs201106962
23andMe	rs201106962
SNPshot	rs201106962
SNPdbe	rs201106962
MSV3d	rs201106962
GWAS Ctlg	rs201106962

Max Magnitude

0

ClinVar
Risk	rs201106962(C;C)
Alt	rs201106962(C;C)
Reference	Rs201106962(A;A)
Significance	Pathogenic
Disease	Parkinson disease 1 Parkinson Disease
Variation	info
Gene	SNCA
CLNDBN	Parkinson disease 1 Parkinson Disease, Dominant
Reversed	0
HGVS	NC_000004.11:g.90749307A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000149507.4, RCV000344706.1,