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rs786205583

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205583(C;C)
Make rs786205583(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position131621897
GeneMED23
is asnp
is mentioned by
dbSNPrs786205583
ebirs786205583
HLIrs786205583
Exacrs786205583
Varsomers786205583
Maprs786205583
PheGenIrs786205583
hapmaprs786205583
1000 genomesrs786205583
hgdprs786205583
ensemblrs786205583
gopubmedrs786205583
geneviewrs786205583
scholarrs786205583
googlers786205583
pharmgkbrs786205583
gwascentralrs786205583
openSNPrs786205583
23andMers786205583
23andMe allrs786205583
SNP Nexus

SNPshotrs786205583
SNPdbers786205583
MSV3drs786205583
GWAS Ctlgrs786205583
Max Magnitude0
ClinVar
Risk rs786205583(C;C)
Alt rs786205583(C;C)
Reference rs786205583(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MED23
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.131943037A>G
CLNSRC
CLNACC RCV000171402.1,