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rs775709247

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs775709247(C;C)
Make rs775709247(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position67802285
GeneZFYVE26
is asnp
is mentioned by
dbSNPrs775709247
dbSNP (classic)rs775709247
ClinGenrs775709247
ebirs775709247
HLIrs775709247
Exacrs775709247
Gnomadrs775709247
Varsomers775709247
LitVarrs775709247
Maprs775709247
PheGenIrs775709247
Biobankrs775709247
1000 genomesrs775709247
hgdprs775709247
ensemblrs775709247
geneviewrs775709247
scholarrs775709247
googlers775709247
pharmgkbrs775709247
gwascentralrs775709247
openSNPrs775709247
23andMers775709247
SNPshotrs775709247
SNPdbers775709247
MSV3drs775709247
GWAS Ctlgrs775709247
Max Magnitude0
ClinVar
Risk rs775709247(C;C)
Alt rs775709247(C;C)
Reference Rs775709247(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ZFYVE26
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.68269002G>C
CLNSRC
CLNACC RCV000493196.1,