rs121908290

Orientation

plus

Stabilized

plus

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

Make rs121908290(G;T)

Make rs121908290(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

109715168

Gene

FIG4

is a	snp
is	mentioned by
dbSNP	rs121908290
dbSNP (classic)	rs121908290
ClinGen	rs121908290
ebi	rs121908290
HLI	rs121908290
Exac	rs121908290
Gnomad	rs121908290
Varsome	rs121908290
LitVar	rs121908290
Map	rs121908290
PheGenI	rs121908290
Biobank	rs121908290
1000 genomes	rs121908290
hgdp	rs121908290
ensembl	rs121908290
geneview	rs121908290
scholar	rs121908290
google	rs121908290
pharmgkb	rs121908290
gwascentral	rs121908290
openSNP	rs121908290
23andMe	rs121908290
SNPshot	rs121908290
SNPdbe	rs121908290
MSV3d	rs121908290
GWAS Ctlg	rs121908290

Max Magnitude

0

OMIM	609390
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121908290(T;T)
Alt	rs121908290(T;T)
Reference	Rs121908290(G;G)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 11
Variation	info
Gene	FIG4
CLNDBN	Amyotrophic lateral sclerosis type 11
Reversed	0
HGVS	NC_000006.11:g.110036371G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001798.3,