rs143781303

Orientation

plus

Stabilized

plus

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

Make rs143781303(C;C)

Make rs143781303(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

68208309

Gene

CLN6

is a	snp
is	mentioned by
dbSNP	rs143781303
dbSNP (classic)	rs143781303
ClinGen	rs143781303
ebi	rs143781303
HLI	rs143781303
Exac	rs143781303
Gnomad	rs143781303
Varsome	rs143781303
LitVar	rs143781303
Map	rs143781303
PheGenI	rs143781303
Biobank	rs143781303
1000 genomes	rs143781303
hgdp	rs143781303
ensembl	rs143781303
geneview	rs143781303
scholar	rs143781303
google	rs143781303
pharmgkb	rs143781303
gwascentral	rs143781303
openSNP	rs143781303
23andMe	rs143781303
SNPshot	rs143781303
SNPdbe	rs143781303
MSV3d	rs143781303
GWAS Ctlg	rs143781303

Max Magnitude

0

ClinVar
Risk	rs143781303(C;C)
Alt	rs143781303(C;C)
Reference	Rs143781303(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CLN6
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.68500647T>C
CLNSRC
CLNACC	RCV000187106.1,