rs774026720

Orientation

plus

Stabilized

plus

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

Make rs774026720(A;A)

Make rs774026720(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

66638273

Gene

KCTD7

is a	snp
is	mentioned by
dbSNP	rs774026720
dbSNP (classic)	rs774026720
ClinGen	rs774026720
ebi	rs774026720
HLI	rs774026720
Exac	rs774026720
Gnomad	rs774026720
Varsome	rs774026720
LitVar	rs774026720
Map	rs774026720
PheGenI	rs774026720
Biobank	rs774026720
1000 genomes	rs774026720
hgdp	rs774026720
ensembl	rs774026720
geneview	rs774026720
scholar	rs774026720
google	rs774026720
pharmgkb	rs774026720
gwascentral	rs774026720
openSNP	rs774026720
23andMe	rs774026720
SNPshot	rs774026720
SNPdbe	rs774026720
MSV3d	rs774026720
GWAS Ctlg	rs774026720

Max Magnitude

0

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,