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rs797045907

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TAGCGGC;TAGCGGC) 0 common in clinvar
Make rs797045907(-;-)
Make rs797045907(-;TAGCGGC)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position116866668
GeneRAD21
is asnp
is mentioned by
dbSNPrs797045907
dbSNP (old)rs797045907
ClinGenrs797045907
ebirs797045907
HLIrs797045907
Exacrs797045907
Gnomadrs797045907
Varsomers797045907
Maprs797045907
PheGenIrs797045907
Biobankrs797045907
1000 genomesrs797045907
hgdprs797045907
ensemblrs797045907
gopubmedrs797045907
geneviewrs797045907
scholarrs797045907
googlers797045907
pharmgkbrs797045907
gwascentralrs797045907
openSNPrs797045907
23andMers797045907
23andMe allrs797045907
SNP Nexus

SNPshotrs797045907
SNPdbers797045907
MSV3drs797045907
GWAS Ctlgrs797045907
Max Magnitude0
ClinVar
Risk rs797045907(-;-)
Alt rs797045907(-;-)
Reference Rs797045907(TAGCGGC;TAGCGGC)
Significance Pathogenic
Disease Cornelia de Lange syndrome 4
Variation info
Gene RAD21
CLNDBN Cornelia de Lange syndrome 4
Reversed 1
HGVS NC_000008.10:g.117878907_117878913delGCCGCTA
CLNSRC
CLNACC RCV000194033.1,