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rs1064794939

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome12
Position115997167
GeneMED13L
is asnp
is mentioned by
dbSNPrs1064794939
dbSNP (old)rs1064794939
ClinGenrs1064794939
ebirs1064794939
HLIrs1064794939
Exacrs1064794939
Gnomadrs1064794939
Varsomers1064794939
Maprs1064794939
PheGenIrs1064794939
Biobankrs1064794939
1000 genomesrs1064794939
hgdprs1064794939
ensemblrs1064794939
gopubmedrs1064794939
geneviewrs1064794939
scholarrs1064794939
googlers1064794939
pharmgkbrs1064794939
gwascentralrs1064794939
openSNPrs1064794939
23andMers1064794939
23andMe allrs1064794939
SNPshotrs1064794939
SNPdbers1064794939
MSV3drs1064794939
GWAS Ctlgrs1064794939
Max Magnitude0
ClinVar
Risk rs1064794939(T;T)
Alt rs1064794939(T;T)
Reference Rs1064794939(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116434972G>A
CLNSRC
CLNACC RCV000480071.1,