rs121908292

Orientation

plus

Stabilized

plus

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

Make rs121908292(G;T)

Make rs121908292(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

77000799

Gene	CLN5, FBXL3

is a	snp
is	mentioned by
dbSNP	rs121908292
dbSNP (classic)	rs121908292
ClinGen	rs121908292
ebi	rs121908292
HLI	rs121908292
Exac	rs121908292
Gnomad	rs121908292
Varsome	rs121908292
LitVar	rs121908292
Map	rs121908292
PheGenI	rs121908292
Biobank	rs121908292
1000 genomes	rs121908292
hgdp	rs121908292
ensembl	rs121908292
geneview	rs121908292
scholar	rs121908292
google	rs121908292
pharmgkb	rs121908292
gwascentral	rs121908292
openSNP	rs121908292
23andMe	rs121908292
SNPshot	rs121908292
SNPdbe	rs121908292
MSV3d	rs121908292
GWAS Ctlg	rs121908292

Max Magnitude

0

OMIM	608102
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121908292(T;T)
Alt	rs121908292(T;T)
Reference	Rs121908292(G;G)
Significance	Other
Disease	Ceroid lipofuscinosis neuronal 5
Variation	info
Gene	CLN5
CLNDBN	Ceroid lipofuscinosis neuronal 5
Reversed	0
HGVS	NC_000013.10:g.77574934G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002677.4,