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rs587784206

From SNPedia

Orientationplus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs587784206(-;-)
Make rs587784206(-;TCT)
Make rs587784206(TCT;TCT)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177293889
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784206
ebirs587784206
HLIrs587784206
Exacrs587784206
Varsomers587784206
Maprs587784206
PheGenIrs587784206
hapmaprs587784206
1000 genomesrs587784206
hgdprs587784206
ensemblrs587784206
gopubmedrs587784206
geneviewrs587784206
scholarrs587784206
googlers587784206
pharmgkbrs587784206
gwascentralrs587784206
openSNPrs587784206
23andMers587784206
23andMe allrs587784206
SNP Nexus

SNPshotrs587784206
SNPdbers587784206
MSV3drs587784206
GWAS Ctlgrs587784206
Max Magnitude0
ClinVar
Risk rs587784206(;)
Alt rs587784206(;)
Reference rs587784206(CTT;CTT)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176720890_176720892delTCT
CLNSRC
CLNACC RCV000146937.1,