rs786205067

Orientation

minus

Stabilized

minus

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

Make rs786205067(-;AACG)

Make rs786205067(AACG;AACG)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

68214315

Gene

CLN6

is a	snp
is	mentioned by
dbSNP	rs786205067
dbSNP (classic)	rs786205067
ClinGen	rs786205067
ebi	rs786205067
HLI	rs786205067
Exac	rs786205067
Gnomad	rs786205067
Varsome	rs786205067
LitVar	rs786205067
Map	rs786205067
PheGenI	rs786205067
Biobank	rs786205067
1000 genomes	rs786205067
hgdp	rs786205067
ensembl	rs786205067
geneview	rs786205067
scholar	rs786205067
google	rs786205067
pharmgkb	rs786205067
gwascentral	rs786205067
openSNP	rs786205067
23andMe	rs786205067
SNPshot	rs786205067
SNPdbe	rs786205067
MSV3d	rs786205067
GWAS Ctlg	rs786205067

Max Magnitude

0

ClinVar
Risk	rs786205067(AACG;AACG)
Alt	rs786205067(AACG;AACG)
Reference	Rs786205067(-;-)
Significance	Pathogenic
Disease	Ceroid lipofuscinosis neuronal 6
Variation	info
Gene	CLN6
CLNDBN	Ceroid lipofuscinosis neuronal 6
Reversed	1
HGVS	NC_000015.9:g.68506654_68506657dupCGTT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004301.5,