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rs878853176

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853176(G;G)
Make rs878853176(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position4815154
GeneITPR1
is asnp
is mentioned by
dbSNPrs878853176
ebirs878853176
HLIrs878853176
Exacrs878853176
Varsomers878853176
Maprs878853176
PheGenIrs878853176
hapmaprs878853176
1000 genomesrs878853176
hgdprs878853176
ensemblrs878853176
gopubmedrs878853176
geneviewrs878853176
scholarrs878853176
googlers878853176
pharmgkbrs878853176
gwascentralrs878853176
openSNPrs878853176
23andMers878853176
23andMe allrs878853176
SNP Nexus

SNPshotrs878853176
SNPdbers878853176
MSV3drs878853176
GWAS Ctlgrs878853176
Max Magnitude0
ClinVar
Risk rs878853176(G;G)
Alt rs878853176(G;G)
Reference rs878853176(T;T)
Significance Pathogenic
Disease Gillespie syndrome
Variation info
Gene ITPR1
CLNDBN Gillespie syndrome
Reversed 0
HGVS NC_000003.11:g.4856838T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000224997.2,