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rs121909540

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909540(A;T)
Make rs121909540(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position20693755
GeneANG, RNASE4
is asnp
is mentioned by
dbSNPrs121909540
ebirs121909540
HLIrs121909540
Exacrs121909540
Varsomers121909540
Maprs121909540
PheGenIrs121909540
hapmaprs121909540
1000 genomesrs121909540
hgdprs121909540
ensemblrs121909540
gopubmedrs121909540
geneviewrs121909540
scholarrs121909540
googlers121909540
pharmgkbrs121909540
gwascentralrs121909540
openSNPrs121909540
23andMers121909540
23andMe allrs121909540
SNP Nexus

SNPshotrs121909540
SNPdbers121909540
MSV3drs121909540
GWAS Ctlgrs121909540
Max Magnitude0
OMIM105850
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909540(T;T)
Alt rs121909540(T;T)
Reference rs121909540(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.21161914A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019704.26,