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rs121909544

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909544(A;A)
Make rs121909544(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position20693973
GeneANG, RNASE4
is asnp
is mentioned by
dbSNPrs121909544
ebirs121909544
HLIrs121909544
Exacrs121909544
Varsomers121909544
Maprs121909544
PheGenIrs121909544
hapmaprs121909544
1000 genomesrs121909544
hgdprs121909544
ensemblrs121909544
gopubmedrs121909544
geneviewrs121909544
scholarrs121909544
googlers121909544
pharmgkbrs121909544
gwascentralrs121909544
openSNPrs121909544
23andMers121909544
23andMe allrs121909544
SNP Nexus

SNPshotrs121909544
SNPdbers121909544
MSV3drs121909544
GWAS Ctlgrs121909544
Max Magnitude0
OMIM105850
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121909544(A;A)
Alt rs121909544(A;A)
Reference rs121909544(G;G)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis type 9
Variation info
Gene ANG RNASE4
CLNDBN Amyotrophic lateral sclerosis type 9
Reversed 0
HGVS NC_000014.8:g.21162132G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019708.27,