rs768091663

Orientation

plus

Stabilized

plus

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

Make rs768091663(C;C)

Make rs768091663(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

20637956

Gene

PINK1

is a	snp
is	mentioned by
dbSNP	rs768091663
dbSNP (classic)	rs768091663
ClinGen	rs768091663
ebi	rs768091663
HLI	rs768091663
Exac	rs768091663
Gnomad	rs768091663
Varsome	rs768091663
LitVar	rs768091663
Map	rs768091663
PheGenI	rs768091663
Biobank	rs768091663
1000 genomes	rs768091663
hgdp	rs768091663
ensembl	rs768091663
geneview	rs768091663
scholar	rs768091663
google	rs768091663
pharmgkb	rs768091663
gwascentral	rs768091663
openSNP	rs768091663
23andMe	rs768091663
SNPshot	rs768091663
SNPdbe	rs768091663
MSV3d	rs768091663
GWAS Ctlg	rs768091663

Max Magnitude

0

ClinVar
Risk	rs768091663(C;C)
Alt	rs768091663(C;C)
Reference	Rs768091663(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PINK1
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.20964449G>C
CLNSRC
CLNACC	RCV000494163.1,