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

rs786205651

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205651(-;-)
Make rs786205651(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position43052526
GeneCUL7
is asnp
is mentioned by
dbSNPrs786205651
ebirs786205651
HLIrs786205651
Exacrs786205651
Varsomers786205651
Maprs786205651
PheGenIrs786205651
hapmaprs786205651
1000 genomesrs786205651
hgdprs786205651
ensemblrs786205651
gopubmedrs786205651
geneviewrs786205651
scholarrs786205651
googlers786205651
pharmgkbrs786205651
gwascentralrs786205651
openSNPrs786205651
23andMers786205651
23andMe allrs786205651
SNP Nexus

SNPshotrs786205651
SNPdbers786205651
MSV3drs786205651
GWAS Ctlgrs786205651
Max Magnitude0
ClinVar
Risk rs786205651(;)
Alt rs786205651(;)
Reference rs786205651(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CUL7
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.43020264delA
CLNSRC
CLNACC RCV000171524.1,