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

rs587784073

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587784073(-;-)
Make rs587784073(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177209855
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784073
ebirs587784073
HLIrs587784073
Exacrs587784073
Varsomers587784073
Maprs587784073
PheGenIrs587784073
hapmaprs587784073
1000 genomesrs587784073
hgdprs587784073
ensemblrs587784073
gopubmedrs587784073
geneviewrs587784073
scholarrs587784073
googlers587784073
pharmgkbrs587784073
gwascentralrs587784073
openSNPrs587784073
23andMers587784073
23andMe allrs587784073
SNP Nexus

SNPshotrs587784073
SNPdbers587784073
MSV3drs587784073
GWAS Ctlgrs587784073
Max Magnitude0
ClinVar
Risk rs587784073(;)
Alt rs587784073(;)
Reference rs587784073(T;T)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176636856delT
CLNSRC
CLNACC RCV000146765.1,