Have questions? Visit https://www.reddit.com/r/SNPedia

rs730880261

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs730880261(-;-)
Make rs730880261(-;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position43038681
GeneCUL7
is asnp
is mentioned by
dbSNPrs730880261
ebirs730880261
HLIrs730880261
Exacrs730880261
Varsomers730880261
Maprs730880261
PheGenIrs730880261
hapmaprs730880261
1000 genomesrs730880261
hgdprs730880261
ensemblrs730880261
gopubmedrs730880261
geneviewrs730880261
scholarrs730880261
googlers730880261
pharmgkbrs730880261
gwascentralrs730880261
openSNPrs730880261
23andMers730880261
23andMe allrs730880261
SNP Nexus

SNPshotrs730880261
SNPdbers730880261
MSV3drs730880261
GWAS Ctlgrs730880261
Max Magnitude0
ClinVar
Risk rs730880261(;)
Alt rs730880261(;)
Reference rs730880261(TG;TG)
Significance Pathogenic
Disease Three M syndrome 1
Variation info
Gene CUL7
CLNDBN Three M syndrome 1
Reversed 1
HGVS NC_000006.11:g.43006419_43006420delCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000001682.4,