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rs1064796611

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTGT;CTGT) 0 common in clinvar
Chromosome12
Position115996558
GeneMED13L
is asnp
is mentioned by
dbSNPrs1064796611
dbSNP (old)rs1064796611
ClinGenrs1064796611
ebirs1064796611
HLIrs1064796611
Exacrs1064796611
Gnomadrs1064796611
Varsomers1064796611
Maprs1064796611
PheGenIrs1064796611
Biobankrs1064796611
1000 genomesrs1064796611
hgdprs1064796611
ensemblrs1064796611
gopubmedrs1064796611
geneviewrs1064796611
scholarrs1064796611
googlers1064796611
pharmgkbrs1064796611
gwascentralrs1064796611
openSNPrs1064796611
23andMers1064796611
23andMe allrs1064796611
SNPshotrs1064796611
SNPdbers1064796611
MSV3drs1064796611
GWAS Ctlgrs1064796611
Max Magnitude0
ClinVar
Risk rs1064796611(-;-)
Alt rs1064796611(-;-)
Reference Rs1064796611(CTGT;CTGT)
Significance Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116434363_116434366delACAG
CLNSRC
CLNACC RCV000481300.1,