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rs587784191

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587784191(A;G)
Make rs587784191(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177292051
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784191
ebirs587784191
HLIrs587784191
Exacrs587784191
Varsomers587784191
Maprs587784191
PheGenIrs587784191
hapmaprs587784191
1000 genomesrs587784191
hgdprs587784191
ensemblrs587784191
gopubmedrs587784191
geneviewrs587784191
scholarrs587784191
googlers587784191
pharmgkbrs587784191
gwascentralrs587784191
openSNPrs587784191
23andMers587784191
23andMe allrs587784191
SNP Nexus

SNPshotrs587784191
SNPdbers587784191
MSV3drs587784191
GWAS Ctlgrs587784191
Max Magnitude0
ClinVar
Risk rs587784191(G;G)
Alt rs587784191(G;G)
Reference rs587784191(A;A)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176719052A>G
CLNSRC
CLNACC RCV000146921.1,