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

rs532007026

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs532007026(C;G)
Make rs532007026(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position25733983
GeneNGLY1
is asnp
is mentioned by
dbSNPrs532007026
dbSNP (classic)rs532007026
ClinGenrs532007026
ebirs532007026
HLIrs532007026
Exacrs532007026
Gnomadrs532007026
Varsomers532007026
LitVarrs532007026
Maprs532007026
PheGenIrs532007026
Biobankrs532007026
1000 genomesrs532007026
hgdprs532007026
ensemblrs532007026
geneviewrs532007026
scholarrs532007026
googlers532007026
pharmgkbrs532007026
gwascentralrs532007026
openSNPrs532007026
23andMers532007026
SNPshotrs532007026
SNPdbers532007026
MSV3drs532007026
GWAS Ctlgrs532007026
Max Magnitude0
ClinVar
Risk rs532007026(G;G)
Alt rs532007026(G;G)
Reference Rs532007026(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NGLY1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.25775474C>G
CLNSRC
CLNACC RCV000413780.1,