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rs587784192

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587784192(-;-)
Make rs587784192(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177292061
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784192
ebirs587784192
HLIrs587784192
Exacrs587784192
Varsomers587784192
Maprs587784192
PheGenIrs587784192
hapmaprs587784192
1000 genomesrs587784192
hgdprs587784192
ensemblrs587784192
gopubmedrs587784192
geneviewrs587784192
scholarrs587784192
googlers587784192
pharmgkbrs587784192
gwascentralrs587784192
openSNPrs587784192
23andMers587784192
23andMe allrs587784192
SNP Nexus

SNPshotrs587784192
SNPdbers587784192
MSV3drs587784192
GWAS Ctlgrs587784192
Max Magnitude0
ClinVar
Risk rs587784192(;)
Alt rs587784192(;)
Reference rs587784192(T;T)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176719062delT
CLNSRC
CLNACC RCV000146922.1,