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rs587784181

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784181(C;T)
Make rs587784181(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177283863
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784181
ebirs587784181
HLIrs587784181
Exacrs587784181
Varsomers587784181
Maprs587784181
PheGenIrs587784181
hapmaprs587784181
1000 genomesrs587784181
hgdprs587784181
ensemblrs587784181
gopubmedrs587784181
geneviewrs587784181
scholarrs587784181
googlers587784181
pharmgkbrs587784181
gwascentralrs587784181
openSNPrs587784181
23andMers587784181
23andMe allrs587784181
SNP Nexus

SNPshotrs587784181
SNPdbers587784181
MSV3drs587784181
GWAS Ctlgrs587784181
Max Magnitude0
ClinVar
Risk rs587784181(T;T)
Alt rs587784181(T;T)
Reference rs587784181(C;C)
Significance Probable-Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176710864C>T
CLNSRC
CLNACC RCV000146910.1,