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rs1057524355

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524355(C;C)
Make rs1057524355(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position201729184
GeneALS2
is asnp
is mentioned by
dbSNPrs1057524355
dbSNP (old)rs1057524355
ClinGenrs1057524355
ebirs1057524355
HLIrs1057524355
Exacrs1057524355
Gnomadrs1057524355
Varsomers1057524355
LitVarrs1057524355
Maprs1057524355
PheGenIrs1057524355
Biobankrs1057524355
1000 genomesrs1057524355
hgdprs1057524355
ensemblrs1057524355
gopubmedrs1057524355
geneviewrs1057524355
scholarrs1057524355
googlers1057524355
pharmgkbrs1057524355
gwascentralrs1057524355
openSNPrs1057524355
23andMers1057524355
23andMe allrs1057524355
SNPshotrs1057524355
SNPdbers1057524355
MSV3drs1057524355
GWAS Ctlgrs1057524355
Max Magnitude0
ClinVar
Risk rs1057524355(C;C)
Alt rs1057524355(C;C)
Reference Rs1057524355(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALS2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.202593907C>G
CLNSRC
CLNACC RCV000426459.1,