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rs121909539

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909539(C;G)
Make rs121909539(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position20693753
GeneANG, RNASE4
is asnp
is mentioned by
dbSNPrs121909539
ebirs121909539
HLIrs121909539
Exacrs121909539
Varsomers121909539
Maprs121909539
PheGenIrs121909539
hapmaprs121909539
1000 genomesrs121909539
hgdprs121909539
ensemblrs121909539
gopubmedrs121909539
geneviewrs121909539
scholarrs121909539
googlers121909539
pharmgkbrs121909539
gwascentralrs121909539
openSNPrs121909539
23andMers121909539
23andMe allrs121909539
SNP Nexus

SNPshotrs121909539
SNPdbers121909539
MSV3drs121909539
GWAS Ctlgrs121909539
Max Magnitude0
OMIM105850
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909539(G;G)
Alt rs121909539(G;G)
Reference rs121909539(C;C)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis type 9
Variation info
Gene RNASE4 ANG
CLNDBN Amyotrophic lateral sclerosis type 9
Reversed 0
HGVS NC_000014.8:g.21161912C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019703.27,