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rs121909536

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909536(A;T)
Make rs121909536(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position20693686
GeneANG, RNASE4
is asnp
is mentioned by
dbSNPrs121909536
ebirs121909536
HLIrs121909536
Exacrs121909536
Varsomers121909536
Maprs121909536
PheGenIrs121909536
hapmaprs121909536
1000 genomesrs121909536
hgdprs121909536
ensemblrs121909536
gopubmedrs121909536
geneviewrs121909536
scholarrs121909536
googlers121909536
pharmgkbrs121909536
gwascentralrs121909536
openSNPrs121909536
23andMers121909536
23andMe allrs121909536
SNP Nexus

SNPshotrs121909536
SNPdbers121909536
MSV3drs121909536
GWAS Ctlgrs121909536
GMAF0.0004591
Max Magnitude0
OMIM105850
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909536(T;T)
Alt rs121909536(T;T)
Reference rs121909536(A;A)
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.21161845A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019700.27,