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rs863225261

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225261(C;C)
Make rs863225261(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position110596431
GeneSMC3
is asnp
is mentioned by
dbSNPrs863225261
ebirs863225261
HLIrs863225261
Exacrs863225261
Varsomers863225261
Maprs863225261
PheGenIrs863225261
hapmaprs863225261
1000 genomesrs863225261
hgdprs863225261
ensemblrs863225261
gopubmedrs863225261
geneviewrs863225261
scholarrs863225261
googlers863225261
pharmgkbrs863225261
gwascentralrs863225261
openSNPrs863225261
23andMers863225261
23andMe allrs863225261
SNP Nexus

SNPshotrs863225261
SNPdbers863225261
MSV3drs863225261
GWAS Ctlgrs863225261
Max Magnitude0
ClinVar
Risk rs863225261(C;C)
Alt rs863225261(C;C)
Reference rs863225261(G;G)
Significance Pathogenic
Disease Cornelia de Lange syndrome 3
Variation info
Gene SMC3
CLNDBN Cornelia de Lange syndrome 3
Reversed 0
HGVS NC_000010.10:g.112356189G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000201859.1,