rs796052688

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(GCGGTCCA;GCGGTCCA)	0	common in clinvar

Make rs796052688(-;-)

Make rs796052688(-;TCCAGCGG)

Make rs796052688(TCCAGCGG;TCCAGCGG)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

66638898

Gene

KCTD7

is a	snp
is	mentioned by
dbSNP	rs796052688
dbSNP (classic)	rs796052688
ClinGen	rs796052688
ebi	rs796052688
HLI	rs796052688
Exac	rs796052688
Gnomad	rs796052688
Varsome	rs796052688
LitVar	rs796052688
Map	rs796052688
PheGenI	rs796052688
Biobank	rs796052688
1000 genomes	rs796052688
hgdp	rs796052688
ensembl	rs796052688
geneview	rs796052688
scholar	rs796052688
google	rs796052688
pharmgkb	rs796052688
gwascentral	rs796052688
openSNP	rs796052688
23andMe	rs796052688
SNPshot	rs796052688
SNPdbe	rs796052688
MSV3d	rs796052688
GWAS Ctlg	rs796052688

Max Magnitude

0

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,