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rs587784167

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587784167(A;A)
Make rs587784167(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177282499
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784167
ebirs587784167
HLIrs587784167
Exacrs587784167
Varsomers587784167
Maprs587784167
PheGenIrs587784167
hapmaprs587784167
1000 genomesrs587784167
hgdprs587784167
ensemblrs587784167
gopubmedrs587784167
geneviewrs587784167
scholarrs587784167
googlers587784167
pharmgkbrs587784167
gwascentralrs587784167
openSNPrs587784167
23andMers587784167
23andMe allrs587784167
SNP Nexus

SNPshotrs587784167
SNPdbers587784167
MSV3drs587784167
GWAS Ctlgrs587784167
Max Magnitude0
ClinVar
Risk rs587784167(A;A)
Alt rs587784167(A;A)
Reference rs587784167(T;T)
Significance Probable-Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176709500T>A
CLNSRC
CLNACC RCV000146896.1,