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rs863224905

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224905(C;C)
Make rs863224905(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position177269601
GeneNSD1
is asnp
is mentioned by
dbSNPrs863224905
ebirs863224905
HLIrs863224905
Exacrs863224905
Varsomers863224905
Maprs863224905
PheGenIrs863224905
hapmaprs863224905
1000 genomesrs863224905
hgdprs863224905
ensemblrs863224905
gopubmedrs863224905
geneviewrs863224905
scholarrs863224905
googlers863224905
pharmgkbrs863224905
gwascentralrs863224905
openSNPrs863224905
23andMers863224905
23andMe allrs863224905
SNP Nexus

SNPshotrs863224905
SNPdbers863224905
MSV3drs863224905
GWAS Ctlgrs863224905
Max Magnitude0
ClinVar
Risk rs863224905(C;C)
Alt rs863224905(C;C)
Reference rs863224905(G;G)
Significance Probable-Pathogenic
Disease Sotos syndrome 1
Variation info
Gene NSD1
CLNDBN Sotos syndrome 1
Reversed 0
HGVS NC_000005.9:g.176696602G>C
CLNSRC
CLNACC RCV000196945.1,