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rs797044934

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044934(C;T)
Make rs797044934(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position201704160
GeneALS2
is asnp
is mentioned by
dbSNPrs797044934
ebirs797044934
HLIrs797044934
Exacrs797044934
Varsomers797044934
Maprs797044934
PheGenIrs797044934
hapmaprs797044934
1000 genomesrs797044934
hgdprs797044934
ensemblrs797044934
gopubmedrs797044934
geneviewrs797044934
scholarrs797044934
googlers797044934
pharmgkbrs797044934
gwascentralrs797044934
openSNPrs797044934
23andMers797044934
23andMe allrs797044934
SNP Nexus

SNPshotrs797044934
SNPdbers797044934
MSV3drs797044934
GWAS Ctlgrs797044934
Max Magnitude0
ClinVar
Risk rs797044934(T;T)
Alt rs797044934(T;T)
Reference rs797044934(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ALS2
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000002.11:g.202568883G>A
CLNSRC
CLNACC RCV000190777.1,