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rs397514761

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514761(C;T)
Make rs397514761(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position39411706
GeneRPSA, SNORA62
is asnp
is mentioned by
dbSNPrs397514761
ebirs397514761
HLIrs397514761
Exacrs397514761
Varsomers397514761
Maprs397514761
PheGenIrs397514761
hapmaprs397514761
1000 genomesrs397514761
hgdprs397514761
ensemblrs397514761
gopubmedrs397514761
geneviewrs397514761
scholarrs397514761
googlers397514761
pharmgkbrs397514761
gwascentralrs397514761
openSNPrs397514761
23andMers397514761
23andMe allrs397514761
SNP Nexus

SNPshotrs397514761
SNPdbers397514761
MSV3drs397514761
GWAS Ctlgrs397514761
Max Magnitude0
ClinVar
Risk rs397514761(T;T)
Alt rs397514761(T;T)
Reference rs397514761(C;C)
Significance Pathogenic
Disease Asplenia
Variation info
Gene SNORA62 RPSA
CLNDBN Asplenia, isolated congenital
Reversed 0
HGVS NC_000003.11:g.39453197C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000054826.22,