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rs121909537

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909537(A;G)
Make rs121909537(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position20693685
GeneANG, RNASE4
is asnp
is mentioned by
dbSNPrs121909537
ebirs121909537
HLIrs121909537
Exacrs121909537
Varsomers121909537
Maprs121909537
PheGenIrs121909537
hapmaprs121909537
1000 genomesrs121909537
hgdprs121909537
ensemblrs121909537
gopubmedrs121909537
geneviewrs121909537
scholarrs121909537
googlers121909537
pharmgkbrs121909537
gwascentralrs121909537
openSNPrs121909537
23andMers121909537
23andMe allrs121909537
SNP Nexus

SNPshotrs121909537
SNPdbers121909537
MSV3drs121909537
GWAS Ctlgrs121909537
Max Magnitude0
OMIM105850
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909537(G;G)
Alt rs121909537(G;G)
Reference rs121909537(A;A)
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.21161844A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019701.27,