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rs587784155

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784155(C;C)
Make rs587784155(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177280683
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784155
ebirs587784155
HLIrs587784155
Exacrs587784155
Varsomers587784155
Maprs587784155
PheGenIrs587784155
hapmaprs587784155
1000 genomesrs587784155
hgdprs587784155
ensemblrs587784155
gopubmedrs587784155
geneviewrs587784155
scholarrs587784155
googlers587784155
pharmgkbrs587784155
gwascentralrs587784155
openSNPrs587784155
23andMers587784155
23andMe allrs587784155
SNP Nexus

SNPshotrs587784155
SNPdbers587784155
MSV3drs587784155
GWAS Ctlgrs587784155
Max Magnitude0
ClinVar
Risk rs587784155(C;C)
Alt rs587784155(C;C)
Reference rs587784155(G;G)
Significance Probable-Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176707684G>C
CLNSRC
CLNACC RCV000146883.1,