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rs587784162

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587784162(C;C)
Make rs587784162(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177280827
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784162
ebirs587784162
HLIrs587784162
Exacrs587784162
Varsomers587784162
Maprs587784162
PheGenIrs587784162
hapmaprs587784162
1000 genomesrs587784162
hgdprs587784162
ensemblrs587784162
gopubmedrs587784162
geneviewrs587784162
scholarrs587784162
googlers587784162
pharmgkbrs587784162
gwascentralrs587784162
openSNPrs587784162
23andMers587784162
23andMe allrs587784162
SNP Nexus

SNPshotrs587784162
SNPdbers587784162
MSV3drs587784162
GWAS Ctlgrs587784162
Max Magnitude0
ClinVar
Risk rs587784162(C;C)
Alt rs587784162(C;C)
Reference rs587784162(T;T)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176707828T>C
CLNSRC
CLNACC RCV000146891.1,