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rs587784168

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784168(G;T)
Make rs587784168(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177282510
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784168
ebirs587784168
HLIrs587784168
Exacrs587784168
Varsomers587784168
Maprs587784168
PheGenIrs587784168
hapmaprs587784168
1000 genomesrs587784168
hgdprs587784168
ensemblrs587784168
gopubmedrs587784168
geneviewrs587784168
scholarrs587784168
googlers587784168
pharmgkbrs587784168
gwascentralrs587784168
openSNPrs587784168
23andMers587784168
23andMe allrs587784168
SNP Nexus

SNPshotrs587784168
SNPdbers587784168
MSV3drs587784168
GWAS Ctlgrs587784168
Max Magnitude0
ClinVar
Risk rs587784168(T;T)
Alt rs587784168(T;T)
Reference rs587784168(G;G)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176709511G>T
CLNSRC
CLNACC RCV000146897.1,