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rs1064793483

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome12
Position116003048
GeneMED13L
is asnp
is mentioned by
dbSNPrs1064793483
dbSNP (old)rs1064793483
ClinGenrs1064793483
ebirs1064793483
HLIrs1064793483
Exacrs1064793483
Gnomadrs1064793483
Varsomers1064793483
Maprs1064793483
PheGenIrs1064793483
Biobankrs1064793483
1000 genomesrs1064793483
hgdprs1064793483
ensemblrs1064793483
gopubmedrs1064793483
geneviewrs1064793483
scholarrs1064793483
googlers1064793483
pharmgkbrs1064793483
gwascentralrs1064793483
openSNPrs1064793483
23andMers1064793483
23andMe allrs1064793483
SNPshotrs1064793483
SNPdbers1064793483
MSV3drs1064793483
GWAS Ctlgrs1064793483
Max Magnitude0
ClinVar
Risk rs1064793483(T;T)
Alt rs1064793483(T;T)
Reference Rs1064793483(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116440853G>A
CLNSRC
CLNACC RCV000481745.1,