rs104894486

Orientation

minus

Stabilized

minus

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

Make rs104894486(C;G)

Make rs104894486(G;G)

Reference

GRCh38 38.1/141

Chromosome

15

Position

68209639

Gene

CLN6

is a	snp
is	mentioned by
dbSNP	rs104894486
dbSNP (classic)	rs104894486
ClinGen	rs104894486
ebi	rs104894486
HLI	rs104894486
Exac	rs104894486
Gnomad	rs104894486
Varsome	rs104894486
LitVar	rs104894486
Map	rs104894486
PheGenI	rs104894486
Biobank	rs104894486
1000 genomes	rs104894486
hgdp	rs104894486
ensembl	rs104894486
geneview	rs104894486
scholar	rs104894486
google	rs104894486
pharmgkb	rs104894486
gwascentral	rs104894486
openSNP	rs104894486
23andMe	rs104894486
SNPshot	rs104894486
SNPdbe	rs104894486
MSV3d	rs104894486
GWAS Ctlg	rs104894486

Max Magnitude

0

OMIM	606725
Desc
Variant	0008
Related	also

ClinVar
Risk	rs104894486(G;G)
Alt	rs104894486(G;G)
Reference	Rs104894486(C;C)
Significance	Pathogenic
Disease	Ceroid lipofuscinosis neuronal 6
Variation	info
Gene	CLN6
CLNDBN	Ceroid lipofuscinosis neuronal 6
Reversed	1
HGVS	NC_000015.9:g.68501977G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004299.3,