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rs774026720

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs774026720(A;A)
Make rs774026720(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position66638273
GeneKCTD7
is asnp
is mentioned by
dbSNPrs774026720
ebirs774026720
HLIrs774026720
Exacrs774026720
Varsomers774026720
Maprs774026720
PheGenIrs774026720
hapmaprs774026720
1000 genomesrs774026720
hgdprs774026720
ensemblrs774026720
gopubmedrs774026720
geneviewrs774026720
scholarrs774026720
googlers774026720
pharmgkbrs774026720
gwascentralrs774026720
openSNPrs774026720
23andMers774026720
23andMe allrs774026720
SNP Nexus

SNPshotrs774026720
SNPdbers774026720
MSV3drs774026720
GWAS Ctlgrs774026720
Max Magnitude0
ClinVar
Risk rs774026720(A;A)
Alt rs774026720(A;A)
Reference rs774026720(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCTD7
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.66103260G>A
CLNSRC
CLNACC RCV000188023.1,