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rs587784209

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784209(C;T)
Make rs587784209(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177293927
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784209
ebirs587784209
HLIrs587784209
Exacrs587784209
Varsomers587784209
Maprs587784209
PheGenIrs587784209
hapmaprs587784209
1000 genomesrs587784209
hgdprs587784209
ensemblrs587784209
gopubmedrs587784209
geneviewrs587784209
scholarrs587784209
googlers587784209
pharmgkbrs587784209
gwascentralrs587784209
openSNPrs587784209
23andMers587784209
23andMe allrs587784209
SNP Nexus

SNPshotrs587784209
SNPdbers587784209
MSV3drs587784209
GWAS Ctlgrs587784209
Max Magnitude0
ClinVar
Risk rs587784209(T;T)
Alt rs587784209(T;T)
Reference rs587784209(C;C)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176720928C>T
CLNSRC
CLNACC RCV000146940.1,