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rs587784097

From SNPedia

Orientationplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs587784097(-;-)
Make rs587784097(-;TG)
Make rs587784097(TG;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177211584
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784097
ebirs587784097
HLIrs587784097
Exacrs587784097
Varsomers587784097
Maprs587784097
PheGenIrs587784097
hapmaprs587784097
1000 genomesrs587784097
hgdprs587784097
ensemblrs587784097
gopubmedrs587784097
geneviewrs587784097
scholarrs587784097
googlers587784097
pharmgkbrs587784097
gwascentralrs587784097
openSNPrs587784097
23andMers587784097
23andMe allrs587784097
SNP Nexus

SNPshotrs587784097
SNPdbers587784097
MSV3drs587784097
GWAS Ctlgrs587784097
Max Magnitude0
ClinVar
Risk rs587784097(;)
Alt rs587784097(;)
Reference rs587784097(GT;GT)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176638585_176638586delTG
CLNSRC
CLNACC RCV000146804.1,