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

rs587784092

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs587784092(-;-)
Make rs587784092(-;CT)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177211353
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784092
ebirs587784092
HLIrs587784092
Exacrs587784092
Varsomers587784092
Maprs587784092
PheGenIrs587784092
hapmaprs587784092
1000 genomesrs587784092
hgdprs587784092
ensemblrs587784092
gopubmedrs587784092
geneviewrs587784092
scholarrs587784092
googlers587784092
pharmgkbrs587784092
gwascentralrs587784092
openSNPrs587784092
23andMers587784092
23andMe allrs587784092
SNP Nexus

SNPshotrs587784092
SNPdbers587784092
MSV3drs587784092
GWAS Ctlgrs587784092
Max Magnitude0
ClinVar
Risk rs587784092(;)
Alt rs587784092(;)
Reference rs587784092(CT;CT)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176638354_176638355delCT
CLNSRC
CLNACC RCV000146796.1,