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rs587784119

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784119(C;G)
Make rs587784119(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177246792
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784119
ebirs587784119
HLIrs587784119
Exacrs587784119
Varsomers587784119
Maprs587784119
PheGenIrs587784119
hapmaprs587784119
1000 genomesrs587784119
hgdprs587784119
ensemblrs587784119
gopubmedrs587784119
geneviewrs587784119
scholarrs587784119
googlers587784119
pharmgkbrs587784119
gwascentralrs587784119
openSNPrs587784119
23andMers587784119
23andMe allrs587784119
SNP Nexus

SNPshotrs587784119
SNPdbers587784119
MSV3drs587784119
GWAS Ctlgrs587784119
Max Magnitude0
ClinVar
Risk rs587784119(G;G)
Alt rs587784119(G;G)
Reference rs587784119(C;C)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176673793C>G
CLNSRC
CLNACC RCV000146837.1,