rs121908080

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(ATC;ATC)	0	common in complete genomics
(I;I)	0	common genotype
(TCA;TCA)	0	common in clinvar

Make rs121908080(-;-)

Make rs121908080(-;ATC)

Reference

GRCh38 38.1/141

Chromosome

15

Position

68211699

Gene

CLN6

is a	snp
is	mentioned by
dbSNP	rs121908080
dbSNP (classic)	rs121908080
ClinGen	rs121908080
ebi	rs121908080
HLI	rs121908080
Exac	rs121908080
Gnomad	rs121908080
Varsome	rs121908080
LitVar	rs121908080
Map	rs121908080
PheGenI	rs121908080
Biobank	rs121908080
1000 genomes	rs121908080
hgdp	rs121908080
ensembl	rs121908080
geneview	rs121908080
scholar	rs121908080
google	rs121908080
pharmgkb	rs121908080
gwascentral	rs121908080
openSNP	rs121908080
23andMe	rs121908080
SNPshot	rs121908080
SNPdbe	rs121908080
MSV3d	rs121908080
GWAS Ctlg	rs121908080

Max Magnitude

0

OMIM	606725
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121908080(-;-)
Alt	rs121908080(-;-)
Reference	Rs121908080(TCA;TCA)
Significance	Pathogenic
Disease	Ceroid lipofuscinosis neuronal 6
Variation	info
Gene	CLN6
CLNDBN	Ceroid lipofuscinosis neuronal 6
Reversed	1
HGVS	NC_000015.9:g.68504037_68504039delGAT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004298.5, RCV000184041.1,