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rs201406974

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs201406974(A;G)
Make rs201406974(G;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position43046304
GeneCUL7
is asnp
is mentioned by
dbSNPrs201406974
ebirs201406974
HLIrs201406974
Exacrs201406974
Varsomers201406974
Maprs201406974
PheGenIrs201406974
hapmaprs201406974
1000 genomesrs201406974
hgdprs201406974
ensemblrs201406974
gopubmedrs201406974
geneviewrs201406974
scholarrs201406974
googlers201406974
pharmgkbrs201406974
gwascentralrs201406974
openSNPrs201406974
23andMers201406974
23andMe allrs201406974
SNP Nexus

SNPshotrs201406974
SNPdbers201406974
MSV3drs201406974
GWAS Ctlgrs201406974
Max Magnitude0
ClinVar
Risk rs201406974(C,G;C,G)
Alt rs201406974(C,G;C,G)
Reference rs201406974(A;A)
Significance Pathogenic
Disease Three M syndrome 1 not provided
Variation info
Gene CUL7
CLNDBN Three M syndrome 1 not provided
Reversed 0
HGVS NC_000006.11:g.43014042A>C
CLNSRC VariO
CLNACC RCV000115042.1, RCV000171523.1,