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rs1064795636

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position127824896
GeneENG, LOC105379841
is asnp
is mentioned by
dbSNPrs1064795636
dbSNP (classic)rs1064795636
ClinGenrs1064795636
ebirs1064795636
HLIrs1064795636
Exacrs1064795636
Gnomadrs1064795636
Varsomers1064795636
LitVarrs1064795636
Maprs1064795636
PheGenIrs1064795636
Biobankrs1064795636
1000 genomesrs1064795636
hgdprs1064795636
ensemblrs1064795636
geneviewrs1064795636
scholarrs1064795636
googlers1064795636
pharmgkbrs1064795636
gwascentralrs1064795636
openSNPrs1064795636
23andMers1064795636
23andMe allrs1064795636
SNPshotrs1064795636
SNPdbers1064795636
MSV3drs1064795636
GWAS Ctlgrs1064795636
Max Magnitude0
ClinVar
Risk rs1064795636(-;-)
Alt rs1064795636(-;-)
Reference Rs1064795636(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ENG
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.130587175delG
CLNSRC
CLNACC RCV000481830.1,