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rs587784166

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784166(G;T)
Make rs587784166(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177282490
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784166
ebirs587784166
HLIrs587784166
Exacrs587784166
Varsomers587784166
Maprs587784166
PheGenIrs587784166
hapmaprs587784166
1000 genomesrs587784166
hgdprs587784166
ensemblrs587784166
gopubmedrs587784166
geneviewrs587784166
scholarrs587784166
googlers587784166
pharmgkbrs587784166
gwascentralrs587784166
openSNPrs587784166
23andMers587784166
23andMe allrs587784166
SNP Nexus

SNPshotrs587784166
SNPdbers587784166
MSV3drs587784166
GWAS Ctlgrs587784166
Max Magnitude0
ClinVar
Risk rs587784166(A,T;A,T)
Alt rs587784166(A,T;A,T)
Reference rs587784166(G;G)
Significance Probable-Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176709491G>T
CLNSRC
CLNACC RCV000146895.1,