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rs587784071

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784071(A;A)
Make rs587784071(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177209661
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784071
ebirs587784071
HLIrs587784071
Exacrs587784071
Varsomers587784071
Maprs587784071
PheGenIrs587784071
hapmaprs587784071
1000 genomesrs587784071
hgdprs587784071
ensemblrs587784071
gopubmedrs587784071
geneviewrs587784071
scholarrs587784071
googlers587784071
pharmgkbrs587784071
gwascentralrs587784071
openSNPrs587784071
23andMers587784071
23andMe allrs587784071
SNP Nexus

SNPshotrs587784071
SNPdbers587784071
MSV3drs587784071
GWAS Ctlgrs587784071
Max Magnitude0
ClinVar
Risk rs587784071(A;A)
Alt rs587784071(A;A)
Reference rs587784071(G;G)
Significance Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176636662G>A
CLNSRC
CLNACC RCV000146762.1,