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rs1064794218

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position127818149
GeneENG, LOC102723566
is asnp
is mentioned by
dbSNPrs1064794218
dbSNP (old)rs1064794218
ClinGenrs1064794218
ebirs1064794218
HLIrs1064794218
Exacrs1064794218
Gnomadrs1064794218
Varsomers1064794218
Maprs1064794218
PheGenIrs1064794218
Biobankrs1064794218
1000 genomesrs1064794218
hgdprs1064794218
ensemblrs1064794218
gopubmedrs1064794218
geneviewrs1064794218
scholarrs1064794218
googlers1064794218
pharmgkbrs1064794218
gwascentralrs1064794218
openSNPrs1064794218
23andMers1064794218
23andMe allrs1064794218
SNPshotrs1064794218
SNPdbers1064794218
MSV3drs1064794218
GWAS Ctlgrs1064794218
Max Magnitude0
ClinVar
Risk rs1064794218(-;-)
Alt rs1064794218(-;-)
Reference Rs1064794218(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ENG LOC102723566
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.130580428delG
CLNSRC
CLNACC RCV000482934.1,