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rs1057518424

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518424(-;A)
Make rs1057518424(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position116008420
GeneMED13L
is asnp
is mentioned by
dbSNPrs1057518424
dbSNP (old)rs1057518424
ClinGenrs1057518424
ebirs1057518424
HLIrs1057518424
Exacrs1057518424
Gnomadrs1057518424
Varsomers1057518424
Maprs1057518424
PheGenIrs1057518424
Biobankrs1057518424
1000 genomesrs1057518424
hgdprs1057518424
ensemblrs1057518424
gopubmedrs1057518424
geneviewrs1057518424
scholarrs1057518424
googlers1057518424
pharmgkbrs1057518424
gwascentralrs1057518424
openSNPrs1057518424
23andMers1057518424
23andMe allrs1057518424
SNPshotrs1057518424
SNPdbers1057518424
MSV3drs1057518424
GWAS Ctlgrs1057518424
Max Magnitude0
ClinVar
Risk rs1057518424(A;A)
Alt rs1057518424(A;A)
Reference Rs1057518424(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116446226dupT
CLNSRC
CLNACC RCV000414148.1,