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rs878853110

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853110(A;A)
Make rs878853110(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position131602382
GeneMED23
is asnp
is mentioned by
dbSNPrs878853110
ebirs878853110
HLIrs878853110
Exacrs878853110
Varsomers878853110
Maprs878853110
PheGenIrs878853110
hapmaprs878853110
1000 genomesrs878853110
hgdprs878853110
ensemblrs878853110
gopubmedrs878853110
geneviewrs878853110
scholarrs878853110
googlers878853110
pharmgkbrs878853110
gwascentralrs878853110
openSNPrs878853110
23andMers878853110
23andMe allrs878853110
SNP Nexus

SNPshotrs878853110
SNPdbers878853110
MSV3drs878853110
GWAS Ctlgrs878853110
Max Magnitude0
ClinVar
Risk rs878853110(A;A)
Alt rs878853110(A;A)
Reference rs878853110(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MED23
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.131923522C>T
CLNSRC
CLNACC RCV000224387.1,