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rs587777118

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777118(C;T)
Make rs587777118(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position92837592
GeneFAM69A, RPL5, SNORD21
is asnp
is mentioned by
dbSNPrs587777118
ebirs587777118
HLIrs587777118
Exacrs587777118
Varsomers587777118
Maprs587777118
PheGenIrs587777118
hapmaprs587777118
1000 genomesrs587777118
hgdprs587777118
ensemblrs587777118
gopubmedrs587777118
geneviewrs587777118
scholarrs587777118
googlers587777118
pharmgkbrs587777118
gwascentralrs587777118
openSNPrs587777118
23andMers587777118
23andMe allrs587777118
SNP Nexus

SNPshotrs587777118
SNPdbers587777118
MSV3drs587777118
GWAS Ctlgrs587777118
Max Magnitude0
ClinVar
Risk rs587777118(T;T)
Alt rs587777118(T;T)
Reference rs587777118(C;C)
Significance Pathogenic
Disease Aase syndrome
Variation info
Gene RPL5 FAM69A SNORD21
CLNDBN Aase syndrome
Reversed 0
HGVS NC_000001.10:g.93303149C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000087039.3,