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rs863225260

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225260(A;A)
Make rs863225260(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position110589944
GeneSMC3
is asnp
is mentioned by
dbSNPrs863225260
ebirs863225260
HLIrs863225260
Exacrs863225260
Varsomers863225260
Maprs863225260
PheGenIrs863225260
hapmaprs863225260
1000 genomesrs863225260
hgdprs863225260
ensemblrs863225260
gopubmedrs863225260
geneviewrs863225260
scholarrs863225260
googlers863225260
pharmgkbrs863225260
gwascentralrs863225260
openSNPrs863225260
23andMers863225260
23andMe allrs863225260
SNP Nexus

SNPshotrs863225260
SNPdbers863225260
MSV3drs863225260
GWAS Ctlgrs863225260
Max Magnitude0
ClinVar
Risk rs863225260(A;A)
Alt rs863225260(A;A)
Reference rs863225260(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.112349702G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000201866.1,