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

rs587784094

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs587784094(-;-)
Make rs587784094(-;GT)
Make rs587784094(GT;GT)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177211445
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784094
ebirs587784094
HLIrs587784094
Exacrs587784094
Varsomers587784094
Maprs587784094
PheGenIrs587784094
hapmaprs587784094
1000 genomesrs587784094
hgdprs587784094
ensemblrs587784094
gopubmedrs587784094
geneviewrs587784094
scholarrs587784094
googlers587784094
pharmgkbrs587784094
gwascentralrs587784094
openSNPrs587784094
23andMers587784094
23andMe allrs587784094
SNP Nexus

SNPshotrs587784094
SNPdbers587784094
MSV3drs587784094
GWAS Ctlgrs587784094
Max Magnitude0
ClinVar
Risk rs587784094(;)
Alt rs587784094(;)
Reference rs587784094(TG;TG)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176638446_176638447delGT
CLNSRC
CLNACC RCV000146799.1,