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rs121434406

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434406(A;A)
Make rs121434406(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position92836283
GeneFAM69A, RPL5
is asnp
is mentioned by
dbSNPrs121434406
ebirs121434406
HLIrs121434406
Exacrs121434406
Varsomers121434406
Maprs121434406
PheGenIrs121434406
hapmaprs121434406
1000 genomesrs121434406
hgdprs121434406
ensemblrs121434406
gopubmedrs121434406
geneviewrs121434406
scholarrs121434406
googlers121434406
pharmgkbrs121434406
gwascentralrs121434406
openSNPrs121434406
23andMers121434406
23andMe allrs121434406
SNP Nexus

SNPshotrs121434406
SNPdbers121434406
MSV3drs121434406
GWAS Ctlgrs121434406
Max Magnitude0
OMIM603634
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434406(A;A)
Alt rs121434406(A;A)
Reference rs121434406(G;G)
Significance Pathogenic
Disease Aase syndrome
Variation info
Gene RPL5 FAM69A SNORD21
CLNDBN Aase syndrome
Reversed 0
HGVS NC_000001.10:g.93301840G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006557.2,