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rs1057524103

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524103(A;A)
Make rs1057524103(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position115997195
GeneMED13L
is asnp
is mentioned by
dbSNPrs1057524103
dbSNP (old)rs1057524103
ClinGenrs1057524103
ebirs1057524103
HLIrs1057524103
Exacrs1057524103
Gnomadrs1057524103
Varsomers1057524103
Maprs1057524103
PheGenIrs1057524103
Biobankrs1057524103
1000 genomesrs1057524103
hgdprs1057524103
ensemblrs1057524103
gopubmedrs1057524103
geneviewrs1057524103
scholarrs1057524103
googlers1057524103
pharmgkbrs1057524103
gwascentralrs1057524103
openSNPrs1057524103
23andMers1057524103
23andMe allrs1057524103
SNPshotrs1057524103
SNPdbers1057524103
MSV3drs1057524103
GWAS Ctlgrs1057524103
Max Magnitude0
ClinVar
Risk rs1057524103(A;A)
Alt rs1057524103(A;A)
Reference Rs1057524103(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116435000G>T
CLNSRC
CLNACC RCV000429083.1,