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rs121909542

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909542(A;A)
Make rs121909542(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position20693719
GeneANG, RNASE4
is asnp
is mentioned by
dbSNPrs121909542
ebirs121909542
HLIrs121909542
Exacrs121909542
Varsomers121909542
Maprs121909542
PheGenIrs121909542
hapmaprs121909542
1000 genomesrs121909542
hgdprs121909542
ensemblrs121909542
gopubmedrs121909542
geneviewrs121909542
scholarrs121909542
googlers121909542
pharmgkbrs121909542
gwascentralrs121909542
openSNPrs121909542
23andMers121909542
23andMe allrs121909542
SNP Nexus

SNPshotrs121909542
SNPdbers121909542
MSV3drs121909542
GWAS Ctlgrs121909542
Max Magnitude0
OMIM105850
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121909542(A,C;A,C)
Alt rs121909542(A,C;A,C)
Reference rs121909542(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.21161878G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019706.27,