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rs1064796732

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TCC;TCC) 0 common in clinvar
Chromosome17
Position13005073
GeneELAC2
is asnp
is mentioned by
dbSNPrs1064796732
dbSNP (old)rs1064796732
ClinGenrs1064796732
ebirs1064796732
HLIrs1064796732
Exacrs1064796732
Gnomadrs1064796732
Varsomers1064796732
Maprs1064796732
PheGenIrs1064796732
Biobankrs1064796732
1000 genomesrs1064796732
hgdprs1064796732
ensemblrs1064796732
gopubmedrs1064796732
geneviewrs1064796732
scholarrs1064796732
googlers1064796732
pharmgkbrs1064796732
gwascentralrs1064796732
openSNPrs1064796732
23andMers1064796732
23andMe allrs1064796732
SNPshotrs1064796732
SNPdbers1064796732
MSV3drs1064796732
GWAS Ctlgrs1064796732
Max Magnitude0
ClinVar
Risk rs1064796732(-;-)
Alt rs1064796732(-;-)
Reference Rs1064796732(TCC;TCC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ELAC2
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.12908390_12908392delGGA
CLNSRC
CLNACC RCV000487244.1,