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rs1057518262

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518262(-;-)
Make rs1057518262(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position115983495
GeneMED13L
is asnp
is mentioned by
dbSNPrs1057518262
dbSNP (old)rs1057518262
ClinGenrs1057518262
ebirs1057518262
HLIrs1057518262
Exacrs1057518262
Gnomadrs1057518262
Varsomers1057518262
Maprs1057518262
PheGenIrs1057518262
Biobankrs1057518262
1000 genomesrs1057518262
hgdprs1057518262
ensemblrs1057518262
gopubmedrs1057518262
geneviewrs1057518262
scholarrs1057518262
googlers1057518262
pharmgkbrs1057518262
gwascentralrs1057518262
openSNPrs1057518262
23andMers1057518262
23andMe allrs1057518262
SNPshotrs1057518262
SNPdbers1057518262
MSV3drs1057518262
GWAS Ctlgrs1057518262
Max Magnitude0
ClinVar
Risk rs1057518262(-;-)
Alt rs1057518262(-;-)
Reference Rs1057518262(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116421300delG
CLNSRC
CLNACC RCV000413201.1,