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rs397515361

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515361(-;-)
Make rs397515361(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position230212372
GeneSP110
is asnp
is mentioned by
dbSNPrs397515361
ebirs397515361
HLIrs397515361
Exacrs397515361
Varsomers397515361
Maprs397515361
PheGenIrs397515361
hapmaprs397515361
1000 genomesrs397515361
hgdprs397515361
ensemblrs397515361
gopubmedrs397515361
geneviewrs397515361
scholarrs397515361
googlers397515361
pharmgkbrs397515361
gwascentralrs397515361
openSNPrs397515361
23andMers397515361
23andMe allrs397515361
SNP Nexus

SNPshotrs397515361
SNPdbers397515361
MSV3drs397515361
GWAS Ctlgrs397515361
Max Magnitude0
ClinVar
Risk rs397515361(;)
Alt rs397515361(;)
Reference rs397515361(C;C)
Significance Pathogenic
Disease Hepatic venoocclusive disease with immunodeficiency
Variation info
Gene SP110 LOC101928789
CLNDBN Hepatic venoocclusive disease with immunodeficiency
Reversed 1
HGVS NC_000002.11:g.231077087delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000005875.4,