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

rs587784132

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784132(G;T)
Make rs587784132(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177257151
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784132
ebirs587784132
HLIrs587784132
Exacrs587784132
Varsomers587784132
Maprs587784132
PheGenIrs587784132
hapmaprs587784132
1000 genomesrs587784132
hgdprs587784132
ensemblrs587784132
gopubmedrs587784132
geneviewrs587784132
scholarrs587784132
googlers587784132
pharmgkbrs587784132
gwascentralrs587784132
openSNPrs587784132
23andMers587784132
23andMe allrs587784132
SNP Nexus

SNPshotrs587784132
SNPdbers587784132
MSV3drs587784132
GWAS Ctlgrs587784132
Max Magnitude0
ClinVar
Risk rs587784132(T;T)
Alt rs587784132(T;T)
Reference rs587784132(G;G)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176684152G>T
CLNSRC
CLNACC RCV000146858.1,