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rs796052688

From SNPedia

Orientationplus
Geno Mag Summary
(GCGGTCCA;GCGGTCCA) 0 common in clinvar
Make rs796052688(-;-)
Make rs796052688(-;TCCAGCGG)
Make rs796052688(TCCAGCGG;TCCAGCGG)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position66638898
GeneKCTD7
is asnp
is mentioned by
dbSNPrs796052688
ebirs796052688
HLIrs796052688
Exacrs796052688
Varsomers796052688
Maprs796052688
PheGenIrs796052688
hapmaprs796052688
1000 genomesrs796052688
hgdprs796052688
ensemblrs796052688
gopubmedrs796052688
geneviewrs796052688
scholarrs796052688
googlers796052688
pharmgkbrs796052688
gwascentralrs796052688
openSNPrs796052688
23andMers796052688
23andMe allrs796052688
SNP Nexus

SNPshotrs796052688
SNPdbers796052688
MSV3drs796052688
GWAS Ctlgrs796052688
Max Magnitude0
ClinVar
Risk rs796052688(;)
Alt rs796052688(;)
Reference rs796052688(GCGGTCCA;GCGGTCCA)
Significance Pathogenic
Disease not provided
Variation info
Gene KCTD7
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.66103885_66103892delTCCAGCGG
CLNSRC
CLNACC RCV000188024.1,