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rs1064796543

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome12
Position115975314
GeneMED13L
is asnp
is mentioned by
dbSNPrs1064796543
dbSNP (old)rs1064796543
ClinGenrs1064796543
ebirs1064796543
HLIrs1064796543
Exacrs1064796543
Gnomadrs1064796543
Varsomers1064796543
Maprs1064796543
PheGenIrs1064796543
Biobankrs1064796543
1000 genomesrs1064796543
hgdprs1064796543
ensemblrs1064796543
gopubmedrs1064796543
geneviewrs1064796543
scholarrs1064796543
googlers1064796543
pharmgkbrs1064796543
gwascentralrs1064796543
openSNPrs1064796543
23andMers1064796543
23andMe allrs1064796543
SNPshotrs1064796543
SNPdbers1064796543
MSV3drs1064796543
GWAS Ctlgrs1064796543
Max Magnitude0
ClinVar
Risk rs1064796543(A;A)
Alt rs1064796543(A;A)
Reference Rs1064796543(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116413119C>T
CLNSRC
CLNACC RCV000487114.1,