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rs397514762

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514762(A;A)
Make rs397514762(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position39408633
GeneRPSA, SNORA6
is asnp
is mentioned by
dbSNPrs397514762
ebirs397514762
HLIrs397514762
Exacrs397514762
Varsomers397514762
Maprs397514762
PheGenIrs397514762
hapmaprs397514762
1000 genomesrs397514762
hgdprs397514762
ensemblrs397514762
gopubmedrs397514762
geneviewrs397514762
scholarrs397514762
googlers397514762
pharmgkbrs397514762
gwascentralrs397514762
openSNPrs397514762
23andMers397514762
23andMe allrs397514762
SNP Nexus

SNPshotrs397514762
SNPdbers397514762
MSV3drs397514762
GWAS Ctlgrs397514762
Max Magnitude0
ClinVar
Risk rs397514762(A;A)
Alt rs397514762(A;A)
Reference rs397514762(C;C)
Significance Pathogenic
Disease Asplenia
Variation info
Gene SNORA6 RPSA
CLNDBN Asplenia, isolated congenital
Reversed 0
HGVS NC_000003.11:g.39450124C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000054827.22,