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rs121909541

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909541(A;G)
Make rs121909541(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position20693772
GeneANG, RNASE4
is asnp
is mentioned by
dbSNPrs121909541
ebirs121909541
HLIrs121909541
Exacrs121909541
Varsomers121909541
Maprs121909541
PheGenIrs121909541
hapmaprs121909541
1000 genomesrs121909541
hgdprs121909541
ensemblrs121909541
gopubmedrs121909541
geneviewrs121909541
scholarrs121909541
googlers121909541
pharmgkbrs121909541
gwascentralrs121909541
openSNPrs121909541
23andMers121909541
23andMe allrs121909541
SNP Nexus

SNPshotrs121909541
SNPdbers121909541
MSV3drs121909541
GWAS Ctlgrs121909541
Max Magnitude0
OMIM105850
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121909541(G;G)
Alt rs121909541(G;G)
Reference rs121909541(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.21161931A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019705.27,