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rs1064795586

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome12
Position115972183
GeneMED13L
is asnp
is mentioned by
dbSNPrs1064795586
dbSNP (classic)rs1064795586
ClinGenrs1064795586
ebirs1064795586
HLIrs1064795586
Exacrs1064795586
Gnomadrs1064795586
Varsomers1064795586
LitVarrs1064795586
Maprs1064795586
PheGenIrs1064795586
Biobankrs1064795586
1000 genomesrs1064795586
hgdprs1064795586
ensemblrs1064795586
geneviewrs1064795586
scholarrs1064795586
googlers1064795586
pharmgkbrs1064795586
gwascentralrs1064795586
openSNPrs1064795586
23andMers1064795586
23andMe allrs1064795586
SNPshotrs1064795586
SNPdbers1064795586
MSV3drs1064795586
GWAS Ctlgrs1064795586
Max Magnitude0
ClinVar
Risk rs1064795586(G;G)
Alt rs1064795586(G;G)
Reference Rs1064795586(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116409988T>C
CLNSRC
CLNACC RCV000482175.1,