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rs587784107

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784107(C;T)
Make rs587784107(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177238279
GeneNSD1
is asnp
is mentioned by
dbSNPrs587784107
dbSNP (classic)rs587784107
ClinGenrs587784107
ebirs587784107
HLIrs587784107
Exacrs587784107
Gnomadrs587784107
Varsomers587784107
LitVarrs587784107
Maprs587784107
PheGenIrs587784107
Biobankrs587784107
1000 genomesrs587784107
hgdprs587784107
ensemblrs587784107
geneviewrs587784107
scholarrs587784107
googlers587784107
pharmgkbrs587784107
gwascentralrs587784107
openSNPrs587784107
23andMers587784107
SNPshotrs587784107
SNPdbers587784107
MSV3drs587784107
GWAS Ctlgrs587784107
Max Magnitude0
ClinVar
Risk rs587784107(T;T)
Alt rs587784107(T;T)
Reference Rs587784107(C;C)
Significance Pathogenic
Disease Sotos syndrome 1 not provided
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1 not provided
Reversed 0
HGVS NC_000005.9:g.176665280C>T
CLNSRC
CLNACC RCV000146821.1, RCV000490145.1,