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rs1064793734

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAGA;AAGA) 0 common in clinvar
Chromosome9
Position127824314
GeneENG, LOC105379841
is asnp
is mentioned by
dbSNPrs1064793734
dbSNP (classic)rs1064793734
ClinGenrs1064793734
ebirs1064793734
HLIrs1064793734
Exacrs1064793734
Gnomadrs1064793734
Varsomers1064793734
LitVarrs1064793734
Maprs1064793734
PheGenIrs1064793734
Biobankrs1064793734
1000 genomesrs1064793734
hgdprs1064793734
ensemblrs1064793734
geneviewrs1064793734
scholarrs1064793734
googlers1064793734
pharmgkbrs1064793734
gwascentralrs1064793734
openSNPrs1064793734
23andMers1064793734
23andMe allrs1064793734
SNPshotrs1064793734
SNPdbers1064793734
MSV3drs1064793734
GWAS Ctlgrs1064793734
Max Magnitude0
ClinVar
Risk rs1064793734(-;-)
Alt rs1064793734(-;-)
Reference Rs1064793734(AAGA;AAGA)
Significance Pathogenic
Disease not provided
Variation info
Gene ENG
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.130586593_130586596delTCTT
CLNSRC
CLNACC RCV000484786.1,