rs796052689

Orientation

plus

Stabilized

plus

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

Make rs796052689(C;C)

Make rs796052689(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

66639066

Gene

KCTD7

is a	snp
is	mentioned by
dbSNP	rs796052689
dbSNP (classic)	rs796052689
ClinGen	rs796052689
ebi	rs796052689
HLI	rs796052689
Exac	rs796052689
Gnomad	rs796052689
Varsome	rs796052689
LitVar	rs796052689
Map	rs796052689
PheGenI	rs796052689
Biobank	rs796052689
1000 genomes	rs796052689
hgdp	rs796052689
ensembl	rs796052689
geneview	rs796052689
scholar	rs796052689
google	rs796052689
pharmgkb	rs796052689
gwascentral	rs796052689
openSNP	rs796052689
23andMe	rs796052689
SNPshot	rs796052689
SNPdbe	rs796052689
MSV3d	rs796052689
GWAS Ctlg	rs796052689

Max Magnitude

0

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,