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rs587784137

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784137(C;T)
Make rs587784137(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177260120
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784137
ebirs587784137
HLIrs587784137
Exacrs587784137
Varsomers587784137
Maprs587784137
PheGenIrs587784137
hapmaprs587784137
1000 genomesrs587784137
hgdprs587784137
ensemblrs587784137
gopubmedrs587784137
geneviewrs587784137
scholarrs587784137
googlers587784137
pharmgkbrs587784137
gwascentralrs587784137
openSNPrs587784137
23andMers587784137
23andMe allrs587784137
SNP Nexus

SNPshotrs587784137
SNPdbers587784137
MSV3drs587784137
GWAS Ctlgrs587784137
Max Magnitude0
ClinVar
Risk rs587784137(T;T)
Alt rs587784137(T;T)
Reference rs587784137(C;C)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176687121C>T
CLNSRC
CLNACC RCV000146863.1,