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rs869312672

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312672(A;A)
Make rs869312672(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position110577847
GeneSMC3
is asnp
is mentioned by
dbSNPrs869312672
ebirs869312672
HLIrs869312672
Exacrs869312672
Varsomers869312672
Maprs869312672
PheGenIrs869312672
hapmaprs869312672
1000 genomesrs869312672
hgdprs869312672
ensemblrs869312672
gopubmedrs869312672
geneviewrs869312672
scholarrs869312672
googlers869312672
pharmgkbrs869312672
gwascentralrs869312672
openSNPrs869312672
23andMers869312672
23andMe allrs869312672
SNP Nexus

SNPshotrs869312672
SNPdbers869312672
MSV3drs869312672
GWAS Ctlgrs869312672
Max Magnitude0
ClinVar
Risk rs869312672(A;A)
Alt rs869312672(A;A)
Reference rs869312672(G;G)
Significance Probable-Pathogenic
Disease Cornelia de Lange syndrome 3
Variation info
Gene SMC3
CLNDBN Cornelia de Lange syndrome 3
Reversed 0
HGVS NC_000010.10:g.112337605G>A
CLNSRC
CLNACC RCV000209912.1,