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rs397514759

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514759(C;T)
Make rs397514759(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position39407678
GeneRPSA, SNORA6
is asnp
is mentioned by
dbSNPrs397514759
ebirs397514759
HLIrs397514759
Exacrs397514759
Varsomers397514759
Maprs397514759
PheGenIrs397514759
hapmaprs397514759
1000 genomesrs397514759
hgdprs397514759
ensemblrs397514759
gopubmedrs397514759
geneviewrs397514759
scholarrs397514759
googlers397514759
pharmgkbrs397514759
gwascentralrs397514759
openSNPrs397514759
23andMers397514759
23andMe allrs397514759
SNP Nexus

SNPshotrs397514759
SNPdbers397514759
MSV3drs397514759
GWAS Ctlgrs397514759
Max Magnitude0
ClinVar
Risk rs397514759(T;T)
Alt rs397514759(T;T)
Reference rs397514759(C;C)
Significance Pathogenic
Disease Asplenia
Variation info
Gene SNORA6 RPSA
CLNDBN Asplenia, isolated congenital
Reversed 0
HGVS NC_000003.11:g.39449169C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000054822.26,