rs769701646

Orientation

plus

Stabilized

plus

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

Make rs769701646(C;T)

Make rs769701646(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

68211754

Gene

CLN6

is a	snp
is	mentioned by
dbSNP	rs769701646
dbSNP (classic)	rs769701646
ClinGen	rs769701646
ebi	rs769701646
HLI	rs769701646
Exac	rs769701646
Gnomad	rs769701646
Varsome	rs769701646
LitVar	rs769701646
Map	rs769701646
PheGenI	rs769701646
Biobank	rs769701646
1000 genomes	rs769701646
hgdp	rs769701646
ensembl	rs769701646
geneview	rs769701646
scholar	rs769701646
google	rs769701646
pharmgkb	rs769701646
gwascentral	rs769701646
openSNP	rs769701646
23andMe	rs769701646
SNPshot	rs769701646
SNPdbe	rs769701646
MSV3d	rs769701646
GWAS Ctlg	rs769701646

Max Magnitude

0

ClinVar
Risk	rs769701646(T;T)
Alt	rs769701646(T;T)
Reference	Rs769701646(C;C)
Significance	Probable-Pathogenic
Disease	Abnormality of brain morphology
Variation	info
Gene	CLN6
CLNDBN	Abnormality of brain morphology
Reversed	0
HGVS	NC_000015.9:g.68504092C>T
CLNSRC
CLNACC	RCV000454168.1,