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rs587784425

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784425(A;A)
Make rs587784425(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position110596398
GeneSMC3
is asnp
is mentioned by
dbSNPrs587784425
ebirs587784425
HLIrs587784425
Exacrs587784425
Varsomers587784425
Maprs587784425
PheGenIrs587784425
hapmaprs587784425
1000 genomesrs587784425
hgdprs587784425
ensemblrs587784425
gopubmedrs587784425
geneviewrs587784425
scholarrs587784425
googlers587784425
pharmgkbrs587784425
gwascentralrs587784425
openSNPrs587784425
23andMers587784425
23andMe allrs587784425
SNP Nexus

SNPshotrs587784425
SNPdbers587784425
MSV3drs587784425
GWAS Ctlgrs587784425
Max Magnitude0
ClinVar
Risk rs587784425(A;A)
Alt rs587784425(A;A)
Reference rs587784425(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.112356156G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000147580.2,