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rs200040003

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200040003(C;T)
Make rs200040003(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position43046583
GeneCUL7
is asnp
is mentioned by
dbSNPrs200040003
ebirs200040003
HLIrs200040003
Exacrs200040003
Varsomers200040003
Maprs200040003
PheGenIrs200040003
hapmaprs200040003
1000 genomesrs200040003
hgdprs200040003
ensemblrs200040003
gopubmedrs200040003
geneviewrs200040003
scholarrs200040003
googlers200040003
pharmgkbrs200040003
gwascentralrs200040003
openSNPrs200040003
23andMers200040003
23andMe allrs200040003
SNP Nexus

SNPshotrs200040003
SNPdbers200040003
MSV3drs200040003
GWAS Ctlgrs200040003
Max Magnitude0
ClinVar
Risk rs200040003(T;T)
Alt rs200040003(T;T)
Reference rs200040003(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CUL7
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.43014321C>T
CLNSRC
CLNACC RCV000171398.1,