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rs397514763

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514763(C;T)
Make rs397514763(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position39408644
GeneRPSA, SNORA6
is asnp
is mentioned by
dbSNPrs397514763
ebirs397514763
HLIrs397514763
Exacrs397514763
Varsomers397514763
Maprs397514763
PheGenIrs397514763
hapmaprs397514763
1000 genomesrs397514763
hgdprs397514763
ensemblrs397514763
gopubmedrs397514763
geneviewrs397514763
scholarrs397514763
googlers397514763
pharmgkbrs397514763
gwascentralrs397514763
openSNPrs397514763
23andMers397514763
23andMe allrs397514763
SNP Nexus

SNPshotrs397514763
SNPdbers397514763
MSV3drs397514763
GWAS Ctlgrs397514763
Max Magnitude0
ClinVar
Risk rs397514763(T;T)
Alt rs397514763(T;T)
Reference rs397514763(C;C)
Significance Pathogenic
Disease Asplenia
Variation info
Gene SNORA6 RPSA
CLNDBN Asplenia, isolated congenital
Reversed 0
HGVS NC_000003.11:g.39450135C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000054828.26,