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rs148890852

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs148890852(C;T)
Make rs148890852(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position36486940
GeneLOC105371749, ZNHIT3
is asnp
is mentioned by
dbSNPrs148890852
dbSNP (old)rs148890852
ClinGenrs148890852
ebirs148890852
HLIrs148890852
Exacrs148890852
Gnomadrs148890852
Varsomers148890852
LitVarrs148890852
Maprs148890852
PheGenIrs148890852
Biobankrs148890852
1000 genomesrs148890852
hgdprs148890852
ensemblrs148890852
gopubmedrs148890852
geneviewrs148890852
scholarrs148890852
googlers148890852
pharmgkbrs148890852
gwascentralrs148890852
openSNPrs148890852
23andMers148890852
23andMe allrs148890852
SNPshotrs148890852
SNPdbers148890852
MSV3drs148890852
GWAS Ctlgrs148890852
Max Magnitude0
ClinVar
Risk rs148890852(T;T)
Alt rs148890852(T;T)
Reference Rs148890852(C;C)
Significance Pathogenic
Disease PEHO syndrome
Variation info
Gene ZNHIT3
CLNDBN PEHO syndrome
Reversed 0
HGVS NC_000017.10:g.34842784C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000490627.1,