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rs752283089

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs752283089(G;T)
Make rs752283089(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position67783217
GeneZFYVE26
is asnp
is mentioned by
dbSNPrs752283089
ebirs752283089
HLIrs752283089
Exacrs752283089
Varsomers752283089
Maprs752283089
PheGenIrs752283089
hapmaprs752283089
1000 genomesrs752283089
hgdprs752283089
ensemblrs752283089
gopubmedrs752283089
geneviewrs752283089
scholarrs752283089
googlers752283089
pharmgkbrs752283089
gwascentralrs752283089
openSNPrs752283089
23andMers752283089
23andMe allrs752283089
SNP Nexus

SNPshotrs752283089
SNPdbers752283089
MSV3drs752283089
GWAS Ctlgrs752283089
Max Magnitude0
ClinVar
Risk rs752283089(T;T)
Alt rs752283089(T;T)
Reference rs752283089(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ZFYVE26
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000014.8:g.68249934G>T
CLNSRC
CLNACC RCV000210539.1,