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rs1064795068

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome12
Position115997164
GeneMED13L
is asnp
is mentioned by
dbSNPrs1064795068
dbSNP (old)rs1064795068
ClinGenrs1064795068
ebirs1064795068
HLIrs1064795068
Exacrs1064795068
Gnomadrs1064795068
Varsomers1064795068
LitVarrs1064795068
Maprs1064795068
PheGenIrs1064795068
Biobankrs1064795068
1000 genomesrs1064795068
hgdprs1064795068
ensemblrs1064795068
gopubmedrs1064795068
geneviewrs1064795068
scholarrs1064795068
googlers1064795068
pharmgkbrs1064795068
gwascentralrs1064795068
openSNPrs1064795068
23andMers1064795068
23andMe allrs1064795068
SNPshotrs1064795068
SNPdbers1064795068
MSV3drs1064795068
GWAS Ctlgrs1064795068
Max Magnitude0
ClinVar
Risk rs1064795068(T;T)
Alt rs1064795068(T;T)
Reference Rs1064795068(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116434969G>A
CLNSRC
CLNACC RCV000483885.1,