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rs1064796113

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome12
Position115983356
GeneMED13L
is asnp
is mentioned by
dbSNPrs1064796113
dbSNP (old)rs1064796113
ClinGenrs1064796113
ebirs1064796113
HLIrs1064796113
Exacrs1064796113
Gnomadrs1064796113
Varsomers1064796113
Maprs1064796113
PheGenIrs1064796113
Biobankrs1064796113
1000 genomesrs1064796113
hgdprs1064796113
ensemblrs1064796113
gopubmedrs1064796113
geneviewrs1064796113
scholarrs1064796113
googlers1064796113
pharmgkbrs1064796113
gwascentralrs1064796113
openSNPrs1064796113
23andMers1064796113
23andMe allrs1064796113
SNPshotrs1064796113
SNPdbers1064796113
MSV3drs1064796113
GWAS Ctlgrs1064796113
Max Magnitude0
ClinVar
Risk rs1064796113(-;-)
Alt rs1064796113(-;-)
Reference Rs1064796113(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116421161delA
CLNSRC
CLNACC RCV000483089.1,