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

rs587784221

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587784221(-;-)
Make rs587784221(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177295411
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784221
ebirs587784221
HLIrs587784221
Exacrs587784221
Varsomers587784221
Maprs587784221
PheGenIrs587784221
hapmaprs587784221
1000 genomesrs587784221
hgdprs587784221
ensemblrs587784221
gopubmedrs587784221
geneviewrs587784221
scholarrs587784221
googlers587784221
pharmgkbrs587784221
gwascentralrs587784221
openSNPrs587784221
23andMers587784221
23andMe allrs587784221
SNP Nexus

SNPshotrs587784221
SNPdbers587784221
MSV3drs587784221
GWAS Ctlgrs587784221
Max Magnitude0
ClinVar
Risk rs587784221(;)
Alt rs587784221(;)
Reference rs587784221(T;T)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176722412delT
CLNSRC
CLNACC RCV000146958.1,