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rs1064794013

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome12
Position116012891
GeneMED13L
is asnp
is mentioned by
dbSNPrs1064794013
dbSNP (old)rs1064794013
ClinGenrs1064794013
ebirs1064794013
HLIrs1064794013
Exacrs1064794013
Gnomadrs1064794013
Varsomers1064794013
LitVarrs1064794013
Maprs1064794013
PheGenIrs1064794013
Biobankrs1064794013
1000 genomesrs1064794013
hgdprs1064794013
ensemblrs1064794013
gopubmedrs1064794013
geneviewrs1064794013
scholarrs1064794013
googlers1064794013
pharmgkbrs1064794013
gwascentralrs1064794013
openSNPrs1064794013
23andMers1064794013
23andMe allrs1064794013
SNPshotrs1064794013
SNPdbers1064794013
MSV3drs1064794013
GWAS Ctlgrs1064794013
Max Magnitude0
ClinVar
Risk rs1064794013(-;-)
Alt rs1064794013(-;-)
Reference Rs1064794013(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116450696delT
CLNSRC
CLNACC RCV000478224.1,