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rs121908290

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908290(G;T)
Make rs121908290(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position109715168
GeneFIG4
is asnp
is mentioned by
dbSNPrs121908290
ebirs121908290
HLIrs121908290
Exacrs121908290
Varsomers121908290
Maprs121908290
PheGenIrs121908290
hapmaprs121908290
1000 genomesrs121908290
hgdprs121908290
ensemblrs121908290
gopubmedrs121908290
geneviewrs121908290
scholarrs121908290
googlers121908290
pharmgkbrs121908290
gwascentralrs121908290
openSNPrs121908290
23andMers121908290
23andMe allrs121908290
SNP Nexus

SNPshotrs121908290
SNPdbers121908290
MSV3drs121908290
GWAS Ctlgrs121908290
Max Magnitude0
OMIM609390
Desc
Variant0008
Relatedalso
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
CLNACC RCV000001798.2,