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rs1057524341

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524341(C;T)
Make rs1057524341(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position115987172
GeneMED13L
is asnp
is mentioned by
dbSNPrs1057524341
dbSNP (old)rs1057524341
ClinGenrs1057524341
ebirs1057524341
HLIrs1057524341
Exacrs1057524341
Gnomadrs1057524341
Varsomers1057524341
LitVarrs1057524341
Maprs1057524341
PheGenIrs1057524341
Biobankrs1057524341
1000 genomesrs1057524341
hgdprs1057524341
ensemblrs1057524341
gopubmedrs1057524341
geneviewrs1057524341
scholarrs1057524341
googlers1057524341
pharmgkbrs1057524341
gwascentralrs1057524341
openSNPrs1057524341
23andMers1057524341
23andMe allrs1057524341
SNPshotrs1057524341
SNPdbers1057524341
MSV3drs1057524341
GWAS Ctlgrs1057524341
Max Magnitude0
ClinVar
Risk rs1057524341(T;T)
Alt rs1057524341(T;T)
Reference Rs1057524341(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116424977G>A
CLNSRC
CLNACC RCV000440181.1,