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

rs1057520573

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520573(A;G)
Make rs1057520573(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position49052426
GeneKMT2D
is asnp
is mentioned by
dbSNPrs1057520573
dbSNP (old)rs1057520573
ClinGenrs1057520573
ebirs1057520573
HLIrs1057520573
Exacrs1057520573
Gnomadrs1057520573
Varsomers1057520573
Maprs1057520573
PheGenIrs1057520573
Biobankrs1057520573
1000 genomesrs1057520573
hgdprs1057520573
ensemblrs1057520573
gopubmedrs1057520573
geneviewrs1057520573
scholarrs1057520573
googlers1057520573
pharmgkbrs1057520573
gwascentralrs1057520573
openSNPrs1057520573
23andMers1057520573
23andMe allrs1057520573
SNPshotrs1057520573
SNPdbers1057520573
MSV3drs1057520573
GWAS Ctlgrs1057520573
Max Magnitude0
ClinVar
Risk rs1057520573(G;G)
Alt rs1057520573(G;G)
Reference Rs1057520573(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KMT2D
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.49446209T>C
CLNSRC
CLNACC RCV000421456.1,