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rs121909538

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909538(A;A)
Make rs121909538(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position20693728
GeneANG, RNASE4
is asnp
is mentioned by
dbSNPrs121909538
ebirs121909538
HLIrs121909538
Exacrs121909538
Varsomers121909538
Maprs121909538
PheGenIrs121909538
hapmaprs121909538
1000 genomesrs121909538
hgdprs121909538
ensemblrs121909538
gopubmedrs121909538
geneviewrs121909538
scholarrs121909538
googlers121909538
pharmgkbrs121909538
gwascentralrs121909538
openSNPrs121909538
23andMers121909538
23andMe allrs121909538
SNP Nexus

SNPshotrs121909538
SNPdbers121909538
MSV3drs121909538
GWAS Ctlgrs121909538
Max Magnitude0
OMIM105850
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909538(A;A)
Alt rs121909538(A;A)
Reference rs121909538(G;G)
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.21161887G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019702.26,