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rs61752334

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61752334(A;C)
Make rs61752334(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position43044883
GeneCUL7
is asnp
is mentioned by
dbSNPrs61752334
ebirs61752334
HLIrs61752334
Exacrs61752334
Varsomers61752334
Maprs61752334
PheGenIrs61752334
hapmaprs61752334
1000 genomesrs61752334
hgdprs61752334
ensemblrs61752334
gopubmedrs61752334
geneviewrs61752334
scholarrs61752334
googlers61752334
pharmgkbrs61752334
gwascentralrs61752334
openSNPrs61752334
23andMers61752334
23andMe allrs61752334
SNP Nexus

SNPshotrs61752334
SNPdbers61752334
MSV3drs61752334
GWAS Ctlgrs61752334
Max Magnitude0
ClinVar
Risk rs61752334(C;C)
Alt rs61752334(C;C)
Reference rs61752334(A;A)
Significance Pathogenic
Disease Three M syndrome 1 Inborn genetic diseases
Variation info
Gene CUL7
CLNDBN Three M syndrome 1 Inborn genetic diseases
Reversed 0
HGVS NC_000006.11:g.43012621A>C
CLNSRC
CLNACC RCV000175080.1, RCV000210570.1,