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rs797044861

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044861(A;C)
Make rs797044861(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position110601742
GeneSMC3
is asnp
is mentioned by
dbSNPrs797044861
ebirs797044861
HLIrs797044861
Exacrs797044861
Varsomers797044861
Maprs797044861
PheGenIrs797044861
hapmaprs797044861
1000 genomesrs797044861
hgdprs797044861
ensemblrs797044861
gopubmedrs797044861
geneviewrs797044861
scholarrs797044861
googlers797044861
pharmgkbrs797044861
gwascentralrs797044861
openSNPrs797044861
23andMers797044861
23andMe allrs797044861
SNP Nexus

SNPshotrs797044861
SNPdbers797044861
MSV3drs797044861
GWAS Ctlgrs797044861
Max Magnitude0
ClinVar
Risk rs797044861(C;C)
Alt rs797044861(C;C)
Reference rs797044861(A;A)
Significance Pathogenic
Disease Inborn genetic diseases Cornelia de Lange syndrome 3
Variation info
Gene SMC3
CLNDBN Inborn genetic diseases Cornelia de Lange syndrome 3
Reversed 0
HGVS NC_000010.10:g.112361500A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000190665.1, RCV000201868.1,