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

rs768176054

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs768176054(-;-)
Make rs768176054(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position67793711
GeneZFYVE26
is asnp
is mentioned by
dbSNPrs768176054
dbSNP (classic)rs768176054
ClinGenrs768176054
ebirs768176054
HLIrs768176054
Exacrs768176054
Gnomadrs768176054
Varsomers768176054
LitVarrs768176054
Maprs768176054
PheGenIrs768176054
Biobankrs768176054
1000 genomesrs768176054
hgdprs768176054
ensemblrs768176054
geneviewrs768176054
scholarrs768176054
googlers768176054
pharmgkbrs768176054
gwascentralrs768176054
openSNPrs768176054
23andMers768176054
SNPshotrs768176054
SNPdbers768176054
MSV3drs768176054
GWAS Ctlgrs768176054
Max Magnitude0
ClinVar
Risk rs768176054(-;-)
Alt rs768176054(-;-)
Reference Rs768176054(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ZFYVE26
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.68260428delA
CLNSRC
CLNACC RCV000494368.1,