Have questions? Visit https://www.reddit.com/r/SNPedia

rs869312914

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312914(C;T)
Make rs869312914(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position67752520
GeneZFYVE26
is asnp
is mentioned by
dbSNPrs869312914
ebirs869312914
HLIrs869312914
Exacrs869312914
Varsomers869312914
Maprs869312914
PheGenIrs869312914
hapmaprs869312914
1000 genomesrs869312914
hgdprs869312914
ensemblrs869312914
gopubmedrs869312914
geneviewrs869312914
scholarrs869312914
googlers869312914
pharmgkbrs869312914
gwascentralrs869312914
openSNPrs869312914
23andMers869312914
23andMe allrs869312914
SNP Nexus

SNPshotrs869312914
SNPdbers869312914
MSV3drs869312914
GWAS Ctlgrs869312914
Max Magnitude0
ClinVar
Risk rs869312914(T;T)
Alt rs869312914(T;T)
Reference rs869312914(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ZFYVE26
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000014.8:g.68219237G>A
CLNSRC
CLNACC RCV000210660.1,