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rs886039506

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039506(C;T)
Make rs886039506(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position127829770
GeneENG, LOC105379841
is asnp
is mentioned by
dbSNPrs886039506
dbSNP (classic)rs886039506
ClinGenrs886039506
ebirs886039506
HLIrs886039506
Exacrs886039506
Gnomadrs886039506
Varsomers886039506
LitVarrs886039506
Maprs886039506
PheGenIrs886039506
Biobankrs886039506
1000 genomesrs886039506
hgdprs886039506
ensemblrs886039506
geneviewrs886039506
scholarrs886039506
googlers886039506
pharmgkbrs886039506
gwascentralrs886039506
openSNPrs886039506
23andMers886039506
SNPshotrs886039506
SNPdbers886039506
MSV3drs886039506
GWAS Ctlgrs886039506
Max Magnitude0
ClinVar
Risk rs886039506(T;T)
Alt rs886039506(T;T)
Reference Rs886039506(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ENG
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.130592049G>A
CLNSRC
CLNACC RCV000255761.1,