rs886039727

Orientation

minus

Stabilized

minus

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

Make rs886039727(A;A)

Make rs886039727(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

15

Position

68218535

Gene

CLN6

is a	snp
is	mentioned by
dbSNP	rs886039727
dbSNP (classic)	rs886039727
ClinGen	rs886039727
ebi	rs886039727
HLI	rs886039727
Exac	rs886039727
Gnomad	rs886039727
Varsome	rs886039727
LitVar	rs886039727
Map	rs886039727
PheGenI	rs886039727
Biobank	rs886039727
1000 genomes	rs886039727
hgdp	rs886039727
ensembl	rs886039727
geneview	rs886039727
scholar	rs886039727
google	rs886039727
pharmgkb	rs886039727
gwascentral	rs886039727
openSNP	rs886039727
23andMe	rs886039727
SNPshot	rs886039727
SNPdbe	rs886039727
MSV3d	rs886039727
GWAS Ctlg	rs886039727

Max Magnitude

0

ClinVar
Risk	rs886039727(A;A)
Alt	rs886039727(A;A)
Reference	Rs886039727(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CLN6
CLNDBN	not provided
Reversed	1
HGVS	NC_000015.9:g.68510873C>T
CLNSRC
CLNACC	RCV000255264.1,