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rs761634625

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GCT;GCT) 0 common in clinvar
Make rs761634625(-;-)
Make rs761634625(-;GCT)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position25737357
GeneNGLY1
is asnp
is mentioned by
dbSNPrs761634625
dbSNP (classic)rs761634625
ClinGenrs761634625
ebirs761634625
HLIrs761634625
Exacrs761634625
Gnomadrs761634625
Varsomers761634625
LitVarrs761634625
Maprs761634625
PheGenIrs761634625
Biobankrs761634625
1000 genomesrs761634625
hgdprs761634625
ensemblrs761634625
geneviewrs761634625
scholarrs761634625
googlers761634625
pharmgkbrs761634625
gwascentralrs761634625
openSNPrs761634625
23andMers761634625
SNPshotrs761634625
SNPdbers761634625
MSV3drs761634625
GWAS Ctlgrs761634625
Max Magnitude0
ClinVar
Risk rs761634625(-;-)
Alt rs761634625(-;-)
Reference Rs761634625(GCT;GCT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NGLY1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.25778848_25778850delGCT
CLNSRC
CLNACC RCV000483669.1,