rs796052345

Orientation

plus

Stabilized

plus

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

Make rs796052345(-;-)

Make rs796052345(-;CT)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

77000959

Gene	CLN5, FBXL3

is a	snp
is	mentioned by
dbSNP	rs796052345
dbSNP (classic)	rs796052345
ClinGen	rs796052345
ebi	rs796052345
HLI	rs796052345
Exac	rs796052345
Gnomad	rs796052345
Varsome	rs796052345
LitVar	rs796052345
Map	rs796052345
PheGenI	rs796052345
Biobank	rs796052345
1000 genomes	rs796052345
hgdp	rs796052345
ensembl	rs796052345
geneview	rs796052345
scholar	rs796052345
google	rs796052345
pharmgkb	rs796052345
gwascentral	rs796052345
openSNP	rs796052345
23andMe	rs796052345
SNPshot	rs796052345
SNPdbe	rs796052345
MSV3d	rs796052345
GWAS Ctlg	rs796052345

Max Magnitude

0

ClinVar
Risk	rs796052345(-;-)
Alt	rs796052345(-;-)
Reference	Rs796052345(CT;CT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CLN5
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.77575094_77575095delCT
CLNSRC
CLNACC	RCV000187074.1,