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rs797044955

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044955(C;T)
Make rs797044955(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position4645673
GeneITPR1
is asnp
is mentioned by
dbSNPrs797044955
ebirs797044955
HLIrs797044955
Exacrs797044955
Varsomers797044955
Maprs797044955
PheGenIrs797044955
hapmaprs797044955
1000 genomesrs797044955
hgdprs797044955
ensemblrs797044955
gopubmedrs797044955
geneviewrs797044955
scholarrs797044955
googlers797044955
pharmgkbrs797044955
gwascentralrs797044955
openSNPrs797044955
23andMers797044955
23andMe allrs797044955
SNP Nexus

SNPshotrs797044955
SNPdbers797044955
MSV3drs797044955
GWAS Ctlgrs797044955
Max Magnitude0
ClinVar
Risk rs797044955(T;T)
Alt rs797044955(T;T)
Reference rs797044955(C;C)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ITPR1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000003.11:g.4687357C>T
CLNSRC
CLNACC RCV000190812.1,