Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057520667

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520667(A;A)
Make rs1057520667(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position49021873
GeneKMT2D
is asnp
is mentioned by
dbSNPrs1057520667
dbSNP (classic)rs1057520667
ClinGenrs1057520667
ebirs1057520667
HLIrs1057520667
Exacrs1057520667
Gnomadrs1057520667
Varsomers1057520667
LitVarrs1057520667
Maprs1057520667
PheGenIrs1057520667
Biobankrs1057520667
1000 genomesrs1057520667
hgdprs1057520667
ensemblrs1057520667
geneviewrs1057520667
scholarrs1057520667
googlers1057520667
pharmgkbrs1057520667
gwascentralrs1057520667
openSNPrs1057520667
23andMers1057520667
23andMe allrs1057520667
SNPshotrs1057520667
SNPdbers1057520667
MSV3drs1057520667
GWAS Ctlgrs1057520667
Max Magnitude0
ClinVar
Risk rs1057520667(A;A)
Alt rs1057520667(A;A)
Reference Rs1057520667(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KMT2D
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.49415656C>T
CLNSRC
CLNACC RCV000428424.1,