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

rs1057518016

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518016(C;T)
Make rs1057518016(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position67797750
GeneZFYVE26
is asnp
is mentioned by
dbSNPrs1057518016
dbSNP (old)rs1057518016
ClinGenrs1057518016
ebirs1057518016
HLIrs1057518016
Exacrs1057518016
Gnomadrs1057518016
Varsomers1057518016
LitVarrs1057518016
Maprs1057518016
PheGenIrs1057518016
Biobankrs1057518016
1000 genomesrs1057518016
hgdprs1057518016
ensemblrs1057518016
gopubmedrs1057518016
geneviewrs1057518016
scholarrs1057518016
googlers1057518016
pharmgkbrs1057518016
gwascentralrs1057518016
openSNPrs1057518016
23andMers1057518016
23andMe allrs1057518016
SNPshotrs1057518016
SNPdbers1057518016
MSV3drs1057518016
GWAS Ctlgrs1057518016
Max Magnitude0
ClinVar
Risk rs1057518016(T;T)
Alt rs1057518016(T;T)
Reference Rs1057518016(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ZFYVE26
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.68264467G>A
CLNSRC
CLNACC RCV000413277.1,