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

rs775407864

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs775407864(A;G)
Make rs775407864(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position148846567
GeneEZH2
is asnp
is mentioned by
dbSNPrs775407864
ebirs775407864
HLIrs775407864
Exacrs775407864
Varsomers775407864
Maprs775407864
PheGenIrs775407864
hapmaprs775407864
1000 genomesrs775407864
hgdprs775407864
ensemblrs775407864
gopubmedrs775407864
geneviewrs775407864
scholarrs775407864
googlers775407864
pharmgkbrs775407864
gwascentralrs775407864
openSNPrs775407864
23andMers775407864
23andMe allrs775407864
SNP Nexus

SNPshotrs775407864
SNPdbers775407864
MSV3drs775407864
GWAS Ctlgrs775407864
Max Magnitude0
ClinVar
Risk rs775407864(G;G)
Alt rs775407864(G;G)
Reference rs775407864(A;A)
Significance Pathogenic
Disease Weaver syndrome
Variation info
Gene EZH2
CLNDBN Weaver syndrome
Reversed 0
HGVS NC_000007.13:g.148543659A>G
CLNSRC
CLNACC RCV000204286.1,