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rs1057520775

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520775(G;T)
Make rs1057520775(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position116277089
GeneMED13L
is asnp
is mentioned by
dbSNPrs1057520775
dbSNP (old)rs1057520775
ClinGenrs1057520775
ebirs1057520775
HLIrs1057520775
Exacrs1057520775
Gnomadrs1057520775
Varsomers1057520775
LitVarrs1057520775
Maprs1057520775
PheGenIrs1057520775
Biobankrs1057520775
1000 genomesrs1057520775
hgdprs1057520775
ensemblrs1057520775
gopubmedrs1057520775
geneviewrs1057520775
scholarrs1057520775
googlers1057520775
pharmgkbrs1057520775
gwascentralrs1057520775
openSNPrs1057520775
23andMers1057520775
23andMe allrs1057520775
SNPshotrs1057520775
SNPdbers1057520775
MSV3drs1057520775
GWAS Ctlgrs1057520775
Max Magnitude0
ClinVar
Risk rs1057520775(T;T)
Alt rs1057520775(T;T)
Reference Rs1057520775(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116714894C>A
CLNSRC
CLNACC RCV000423089.1,