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rs587784196

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587784196(A;G)
Make rs587784196(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177292113
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784196
ebirs587784196
HLIrs587784196
Exacrs587784196
Varsomers587784196
Maprs587784196
PheGenIrs587784196
hapmaprs587784196
1000 genomesrs587784196
hgdprs587784196
ensemblrs587784196
gopubmedrs587784196
geneviewrs587784196
scholarrs587784196
googlers587784196
pharmgkbrs587784196
gwascentralrs587784196
openSNPrs587784196
23andMers587784196
23andMe allrs587784196
SNP Nexus

SNPshotrs587784196
SNPdbers587784196
MSV3drs587784196
GWAS Ctlgrs587784196
Max Magnitude0
ClinVar
Risk rs587784196(G;G)
Alt rs587784196(G;G)
Reference rs587784196(A;A)
Significance Probable-Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176719114A>G
CLNSRC
CLNACC RCV000146926.1,