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rs587784122

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784122(C;T)
Make rs587784122(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177251769
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784122
ClinGenrs587784122
ebirs587784122
HLIrs587784122
Exacrs587784122
Varsomers587784122
Maprs587784122
PheGenIrs587784122
hapmaprs587784122
1000 genomesrs587784122
hgdprs587784122
ensemblrs587784122
gopubmedrs587784122
geneviewrs587784122
scholarrs587784122
googlers587784122
pharmgkbrs587784122
gwascentralrs587784122
openSNPrs587784122
23andMers587784122
23andMe allrs587784122
SNP Nexus

SNPshotrs587784122
SNPdbers587784122
MSV3drs587784122
GWAS Ctlgrs587784122
Max Magnitude0
ClinVar
Risk rs587784122(T;T)
Alt rs587784122(T;T)
Reference Rs587784122(C;C)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176678770C>T
CLNSRC
CLNACC RCV000146844.1,