rs121908079

Orientation

minus

Stabilized

minus

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

Make rs121908079(-;-)

Make rs121908079(-;TAT)

Reference

GRCh38 38.1/141

Chromosome

15

Position

68211292

Gene

CLN6

is a	snp
is	mentioned by
dbSNP	rs121908079
dbSNP (classic)	rs121908079
ClinGen	rs121908079
ebi	rs121908079
HLI	rs121908079
Exac	rs121908079
Gnomad	rs121908079
Varsome	rs121908079
LitVar	rs121908079
Map	rs121908079
PheGenI	rs121908079
Biobank	rs121908079
1000 genomes	rs121908079
hgdp	rs121908079
ensembl	rs121908079
geneview	rs121908079
scholar	rs121908079
google	rs121908079
pharmgkb	rs121908079
gwascentral	rs121908079
openSNP	rs121908079
23andMe	rs121908079
SNPshot	rs121908079
SNPdbe	rs121908079
MSV3d	rs121908079
GWAS Ctlg	rs121908079

Max Magnitude

0

OMIM	606725
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121908079(-;-)
Alt	rs121908079(-;-)
Reference	Rs121908079(TAT;TAT)
Significance	Pathogenic
Disease	Ceroid lipofuscinosis neuronal 6
Variation	info
Gene	CLN6
CLNDBN	Ceroid lipofuscinosis neuronal 6
Reversed	1
HGVS	NC_000015.9:g.68503630_68503632delATA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004293.3,