rs1060499619

Orientation

minus

Stabilized

minus

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

Make rs1060499619(C;C)

Make rs1060499619(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

21

Position

32681590

Gene

SYNJ1

is a	snp
is	mentioned by
dbSNP	rs1060499619
dbSNP (classic)	rs1060499619
ClinGen	rs1060499619
ebi	rs1060499619
HLI	rs1060499619
Exac	rs1060499619
Gnomad	rs1060499619
Varsome	rs1060499619
LitVar	rs1060499619
Map	rs1060499619
PheGenI	rs1060499619
Biobank	rs1060499619
1000 genomes	rs1060499619
hgdp	rs1060499619
ensembl	rs1060499619
geneview	rs1060499619
scholar	rs1060499619
google	rs1060499619
pharmgkb	rs1060499619
gwascentral	rs1060499619
openSNP	rs1060499619
23andMe	rs1060499619
SNPshot	rs1060499619
SNPdbe	rs1060499619
MSV3d	rs1060499619
GWAS Ctlg	rs1060499619

Max Magnitude

0

ClinVar
Risk	rs1060499619(C;C)
Alt	rs1060499619(C;C)
Reference	Rs1060499619(G;G)
Significance	Pathogenic
Disease	Parkinson disease 20
Variation	info
Gene	SYNJ1
CLNDBN	Parkinson disease 20, early-onset
Reversed	1
HGVS	NC_000021.8:g.34053900C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000445361.1,