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rs879255407

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879255407(-;-)
Make rs879255407(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position115975659
GeneMED13L
is asnp
is mentioned by
dbSNPrs879255407
ebirs879255407
HLIrs879255407
Exacrs879255407
Varsomers879255407
Maprs879255407
PheGenIrs879255407
hapmaprs879255407
1000 genomesrs879255407
hgdprs879255407
ensemblrs879255407
gopubmedrs879255407
geneviewrs879255407
scholarrs879255407
googlers879255407
pharmgkbrs879255407
gwascentralrs879255407
openSNPrs879255407
23andMers879255407
23andMe allrs879255407
SNP Nexus

SNPshotrs879255407
SNPdbers879255407
MSV3drs879255407
GWAS Ctlgrs879255407
Max Magnitude0
ClinVar
Risk rs879255407(;)
Alt rs879255407(;)
Reference rs879255407(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MED13L
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.116413464delG
CLNSRC
CLNACC RCV000239101.1,