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

rs587784158

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784158(A;A)
Make rs587784158(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177280747
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784158
ebirs587784158
HLIrs587784158
Exacrs587784158
Varsomers587784158
Maprs587784158
PheGenIrs587784158
hapmaprs587784158
1000 genomesrs587784158
hgdprs587784158
ensemblrs587784158
gopubmedrs587784158
geneviewrs587784158
scholarrs587784158
googlers587784158
pharmgkbrs587784158
gwascentralrs587784158
openSNPrs587784158
23andMers587784158
23andMe allrs587784158
SNP Nexus

SNPshotrs587784158
SNPdbers587784158
MSV3drs587784158
GWAS Ctlgrs587784158
Max Magnitude0
ClinVar
Risk rs587784158(A;A)
Alt rs587784158(A;A)
Reference rs587784158(C;C)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176707748C>A
CLNSRC
CLNACC RCV000146887.1,