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rs397514760

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514760(C;G)
Make rs397514760(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position39411688
GeneRPSA, SNORA62
is asnp
is mentioned by
dbSNPrs397514760
ebirs397514760
HLIrs397514760
Exacrs397514760
Varsomers397514760
Maprs397514760
PheGenIrs397514760
hapmaprs397514760
1000 genomesrs397514760
hgdprs397514760
ensemblrs397514760
gopubmedrs397514760
geneviewrs397514760
scholarrs397514760
googlers397514760
pharmgkbrs397514760
gwascentralrs397514760
openSNPrs397514760
23andMers397514760
23andMe allrs397514760
SNP Nexus

SNPshotrs397514760
SNPdbers397514760
MSV3drs397514760
GWAS Ctlgrs397514760
Max Magnitude0
ClinVar
Risk rs397514760(G,T;G,T)
Alt rs397514760(G,T;G,T)
Reference rs397514760(C;C)
Significance Pathogenic
Disease Asplenia
Variation info
Gene SNORA62 RPSA
CLNDBN Asplenia, isolated congenital
Reversed 0
HGVS NC_000003.11:g.39453179C>G; NC_000003.11:g.39453179C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000054824.26, RCV000054825.26,