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rs1057520056

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520056(A;A)
Make rs1057520056(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position115997209
GeneMED13L
is asnp
is mentioned by
dbSNPrs1057520056
dbSNP (old)rs1057520056
ClinGenrs1057520056
ebirs1057520056
HLIrs1057520056
Exacrs1057520056
Gnomadrs1057520056
Varsomers1057520056
Maprs1057520056
PheGenIrs1057520056
Biobankrs1057520056
1000 genomesrs1057520056
hgdprs1057520056
ensemblrs1057520056
gopubmedrs1057520056
geneviewrs1057520056
scholarrs1057520056
googlers1057520056
pharmgkbrs1057520056
gwascentralrs1057520056
openSNPrs1057520056
23andMers1057520056
23andMe allrs1057520056
SNPshotrs1057520056
SNPdbers1057520056
MSV3drs1057520056
GWAS Ctlgrs1057520056
Max Magnitude0
ClinVar
Risk rs1057520056(A;A)
Alt rs1057520056(A;A)
Reference Rs1057520056(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116435014A>T
CLNSRC
CLNACC RCV000427272.1,