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rs121909535

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909535(A;T)
Make rs121909535(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position20693671
GeneANG, RNASE4
is asnp
is mentioned by
dbSNPrs121909535
ebirs121909535
HLIrs121909535
Exacrs121909535
Varsomers121909535
Maprs121909535
PheGenIrs121909535
hapmaprs121909535
1000 genomesrs121909535
hgdprs121909535
ensemblrs121909535
gopubmedrs121909535
geneviewrs121909535
scholarrs121909535
googlers121909535
pharmgkbrs121909535
gwascentralrs121909535
openSNPrs121909535
23andMers121909535
23andMe allrs121909535
SNP Nexus

SNPshotrs121909535
SNPdbers121909535
MSV3drs121909535
GWAS Ctlgrs121909535
Max Magnitude0
OMIM105850
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909535(T;T)
Alt rs121909535(T;T)
Reference Rs121909535(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.21161830A>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000019699.27,