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

rs796052689

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052689(C;C)
Make rs796052689(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position66639066
GeneKCTD7
is asnp
is mentioned by
dbSNPrs796052689
ebirs796052689
HLIrs796052689
Exacrs796052689
Varsomers796052689
Maprs796052689
PheGenIrs796052689
hapmaprs796052689
1000 genomesrs796052689
hgdprs796052689
ensemblrs796052689
gopubmedrs796052689
geneviewrs796052689
scholarrs796052689
googlers796052689
pharmgkbrs796052689
gwascentralrs796052689
openSNPrs796052689
23andMers796052689
23andMe allrs796052689
SNP Nexus

SNPshotrs796052689
SNPdbers796052689
MSV3drs796052689
GWAS Ctlgrs796052689
Max Magnitude0
ClinVar
Risk rs796052689(C;C)
Alt rs796052689(C;C)
Reference rs796052689(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCTD7
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.66104053G>C
CLNSRC
CLNACC RCV000188025.2,