rs546989392

Orientation

plus

Stabilized

plus

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

Make rs546989392(C;T)

Make rs546989392(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

76996010

Gene	CLN5, FBXL3

is a	snp
is	mentioned by
dbSNP	rs546989392
dbSNP (classic)	rs546989392
ClinGen	rs546989392
ebi	rs546989392
HLI	rs546989392
Exac	rs546989392
Gnomad	rs546989392
Varsome	rs546989392
LitVar	rs546989392
Map	rs546989392
PheGenI	rs546989392
Biobank	rs546989392
1000 genomes	rs546989392
hgdp	rs546989392
ensembl	rs546989392
geneview	rs546989392
scholar	rs546989392
google	rs546989392
pharmgkb	rs546989392
gwascentral	rs546989392
openSNP	rs546989392
23andMe	rs546989392
SNPshot	rs546989392
SNPdbe	rs546989392
MSV3d	rs546989392
GWAS Ctlg	rs546989392

Max Magnitude

0

ClinVar
Risk	rs546989392(T;T)
Alt	rs546989392(T;T)
Reference	Rs546989392(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CLN5
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.77570145C>T
CLNSRC
CLNACC	RCV000187069.1,