rs199624315

Orientation

plus

Stabilized

plus

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

Make rs199624315(G;T)

Make rs199624315(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

66638300

Gene

KCTD7

is a	snp
is	mentioned by
dbSNP	rs199624315
dbSNP (classic)	rs199624315
ClinGen	rs199624315
ebi	rs199624315
HLI	rs199624315
Exac	rs199624315
Gnomad	rs199624315
Varsome	rs199624315
LitVar	rs199624315
Map	rs199624315
PheGenI	rs199624315
Biobank	rs199624315
1000 genomes	rs199624315
hgdp	rs199624315
ensembl	rs199624315
geneview	rs199624315
scholar	rs199624315
google	rs199624315
pharmgkb	rs199624315
gwascentral	rs199624315
openSNP	rs199624315
23andMe	rs199624315
SNPshot	rs199624315
SNPdbe	rs199624315
MSV3d	rs199624315
GWAS Ctlg	rs199624315

Max Magnitude

0

ClinVar
Risk	rs199624315(A;A) rs199624315(T;T)
Alt	rs199624315(A;A) rs199624315(T;T)
Reference	Rs199624315(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCTD7
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.66103287G>T
CLNSRC
CLNACC	RCV000188028.1,