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rs587784157

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784157(C;T)
Make rs587784157(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177280742
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784157
ebirs587784157
HLIrs587784157
Exacrs587784157
Varsomers587784157
Maprs587784157
PheGenIrs587784157
hapmaprs587784157
1000 genomesrs587784157
hgdprs587784157
ensemblrs587784157
gopubmedrs587784157
geneviewrs587784157
scholarrs587784157
googlers587784157
pharmgkbrs587784157
gwascentralrs587784157
openSNPrs587784157
23andMers587784157
23andMe allrs587784157
SNP Nexus

SNPshotrs587784157
SNPdbers587784157
MSV3drs587784157
GWAS Ctlgrs587784157
Max Magnitude0
ClinVar
Risk rs587784157(T;T)
Alt rs587784157(T;T)
Reference rs587784157(C;C)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176707743C>T
CLNSRC
CLNACC RCV000146886.1,