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rs397515548

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515548(A;A)
Make rs397515548(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position148807669
GeneEZH2
is asnp
is mentioned by
dbSNPrs397515548
ebirs397515548
HLIrs397515548
Exacrs397515548
Varsomers397515548
Maprs397515548
PheGenIrs397515548
hapmaprs397515548
1000 genomesrs397515548
hgdprs397515548
ensemblrs397515548
gopubmedrs397515548
geneviewrs397515548
scholarrs397515548
googlers397515548
pharmgkbrs397515548
gwascentralrs397515548
openSNPrs397515548
23andMers397515548
23andMe allrs397515548
SNP Nexus

SNPshotrs397515548
SNPdbers397515548
MSV3drs397515548
GWAS Ctlgrs397515548
Max Magnitude0
ClinVar
Risk rs397515548(A;A)
Alt rs397515548(A;A)
Reference rs397515548(G;G)
Significance Pathogenic
Disease Weaver syndrome
Variation info
Gene EZH2
CLNDBN Weaver syndrome
Reversed 1
HGVS NC_000007.13:g.148504761C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000055901.1,