rs750811871

Orientation

plus

Stabilized

plus

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

Make rs750811871(C;T)

Make rs750811871(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

66638993

Gene

KCTD7

is a	snp
is	mentioned by
dbSNP	rs750811871
dbSNP (classic)	rs750811871
ClinGen	rs750811871
ebi	rs750811871
HLI	rs750811871
Exac	rs750811871
Gnomad	rs750811871
Varsome	rs750811871
LitVar	rs750811871
Map	rs750811871
PheGenI	rs750811871
Biobank	rs750811871
1000 genomes	rs750811871
hgdp	rs750811871
ensembl	rs750811871
geneview	rs750811871
scholar	rs750811871
google	rs750811871
pharmgkb	rs750811871
gwascentral	rs750811871
openSNP	rs750811871
23andMe	rs750811871
SNPshot	rs750811871
SNPdbe	rs750811871
MSV3d	rs750811871
GWAS Ctlg	rs750811871

Max Magnitude

0

ClinVar
Risk	rs750811871(T;T)
Alt	rs750811871(T;T)
Reference	Rs750811871(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCTD7
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.66103980C>T
CLNSRC
CLNACC	RCV000426305.1,