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rs587784429

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784429(C;C)
Make rs587784429(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position110582082
GeneSMC3
is asnp
is mentioned by
dbSNPrs587784429
ebirs587784429
HLIrs587784429
Exacrs587784429
Varsomers587784429
Maprs587784429
PheGenIrs587784429
hapmaprs587784429
1000 genomesrs587784429
hgdprs587784429
ensemblrs587784429
gopubmedrs587784429
geneviewrs587784429
scholarrs587784429
googlers587784429
pharmgkbrs587784429
gwascentralrs587784429
openSNPrs587784429
23andMers587784429
23andMe allrs587784429
SNP Nexus

SNPshotrs587784429
SNPdbers587784429
MSV3drs587784429
GWAS Ctlgrs587784429
Max Magnitude0
ClinVar
Risk rs587784429(C;C)
Alt rs587784429(C;C)
Reference rs587784429(G;G)
Significance Other
Disease Cornelia de Lange syndrome 3
Variation info
Gene SMC3
CLNDBN Cornelia de Lange syndrome 3
Reversed 0
HGVS NC_000010.10:g.112341840G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000147600.2,