Have questions? Visit https://www.reddit.com/r/SNPedia

rs761291489

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs761291489(C;T)
Make rs761291489(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position201711091
GeneALS2
is asnp
is mentioned by
dbSNPrs761291489
dbSNP (classic)rs761291489
ClinGenrs761291489
ebirs761291489
HLIrs761291489
Exacrs761291489
Gnomadrs761291489
Varsomers761291489
LitVarrs761291489
Maprs761291489
PheGenIrs761291489
Biobankrs761291489
1000 genomesrs761291489
hgdprs761291489
ensemblrs761291489
geneviewrs761291489
scholarrs761291489
googlers761291489
pharmgkbrs761291489
gwascentralrs761291489
openSNPrs761291489
23andMers761291489
23andMe allrs761291489
SNPshotrs761291489
SNPdbers761291489
MSV3drs761291489
GWAS Ctlgrs761291489
Max Magnitude0
ClinVar
Risk rs761291489(T;T)
Alt rs761291489(T;T)
Reference Rs761291489(C;C)
Significance Probable-Pathogenic
Disease Peripheral axonal neuropathy
Variation info
Gene ALS2
CLNDBN Peripheral axonal neuropathy
Reversed 0
HGVS NC_000002.11:g.202575814C>T
CLNSRC
CLNACC RCV000415216.1,