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rs786205478

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205478(C;T)
Make rs786205478(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position49033310
GeneKMT2D
is asnp
is mentioned by
dbSNPrs786205478
ebirs786205478
HLIrs786205478
Exacrs786205478
Varsomers786205478
Maprs786205478
PheGenIrs786205478
hapmaprs786205478
1000 genomesrs786205478
hgdprs786205478
ensemblrs786205478
gopubmedrs786205478
geneviewrs786205478
scholarrs786205478
googlers786205478
pharmgkbrs786205478
gwascentralrs786205478
openSNPrs786205478
23andMers786205478
23andMe allrs786205478
SNP Nexus

SNPshotrs786205478
SNPdbers786205478
MSV3drs786205478
GWAS Ctlgrs786205478
Max Magnitude0
ClinVar
Risk rs786205478(T;T)
Alt rs786205478(T;T)
Reference rs786205478(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2D
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.49427093G>A
CLNSRC
CLNACC RCV000171213.1,