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rs864321657

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864321657(C;T)
Make rs864321657(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position9448586
GeneSETD5
is asnp
is mentioned by
dbSNPrs864321657
ebirs864321657
HLIrs864321657
Exacrs864321657
Varsomers864321657
Maprs864321657
PheGenIrs864321657
hapmaprs864321657
1000 genomesrs864321657
hgdprs864321657
ensemblrs864321657
gopubmedrs864321657
geneviewrs864321657
scholarrs864321657
googlers864321657
pharmgkbrs864321657
gwascentralrs864321657
openSNPrs864321657
23andMers864321657
23andMe allrs864321657
SNP Nexus

SNPshotrs864321657
SNPdbers864321657
MSV3drs864321657
GWAS Ctlgrs864321657
Max Magnitude0
ClinVar
Risk rs864321657(T;T)
Alt rs864321657(T;T)
Reference rs864321657(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene SETD5
CLNDBN Mental retardation, autosomal dominant 23
Reversed 0
HGVS NC_000003.11:g.9490270C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000203577.1,