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rs730880262

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs730880262(-;-)
Make rs730880262(-;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position43043156
GeneCUL7
is asnp
is mentioned by
dbSNPrs730880262
ebirs730880262
HLIrs730880262
Exacrs730880262
Varsomers730880262
Maprs730880262
PheGenIrs730880262
hapmaprs730880262
1000 genomesrs730880262
hgdprs730880262
ensemblrs730880262
gopubmedrs730880262
geneviewrs730880262
scholarrs730880262
googlers730880262
pharmgkbrs730880262
gwascentralrs730880262
openSNPrs730880262
23andMers730880262
23andMe allrs730880262
SNP Nexus

SNPshotrs730880262
SNPdbers730880262
MSV3drs730880262
GWAS Ctlgrs730880262
Max Magnitude0
ClinVar
Risk rs730880262(;)
Alt rs730880262(;)
Reference rs730880262(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.43010894_43010895delCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000001685.3,