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

rs786205581

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205581(G;T)
Make rs786205581(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position43038604
GeneCUL7
is asnp
is mentioned by
dbSNPrs786205581
ebirs786205581
HLIrs786205581
Exacrs786205581
Varsomers786205581
Maprs786205581
PheGenIrs786205581
hapmaprs786205581
1000 genomesrs786205581
hgdprs786205581
ensemblrs786205581
gopubmedrs786205581
geneviewrs786205581
scholarrs786205581
googlers786205581
pharmgkbrs786205581
gwascentralrs786205581
openSNPrs786205581
23andMers786205581
23andMe allrs786205581
SNP Nexus

SNPshotrs786205581
SNPdbers786205581
MSV3drs786205581
GWAS Ctlgrs786205581
Max Magnitude0
ClinVar
Risk rs786205581(T;T)
Alt rs786205581(T;T)
Reference rs786205581(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CUL7
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.43006342C>A
CLNSRC
CLNACC RCV000171397.1,