rs200040003

Orientation

plus

Stabilized

plus

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

Make rs200040003(C;T)

Make rs200040003(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

43046583

Gene

CUL7

is a	snp
is	mentioned by
dbSNP	rs200040003
dbSNP (classic)	rs200040003
ClinGen	rs200040003
ebi	rs200040003
HLI	rs200040003
Exac	rs200040003
Gnomad	rs200040003
Varsome	rs200040003
LitVar	rs200040003
Map	rs200040003
PheGenI	rs200040003
Biobank	rs200040003
1000 genomes	rs200040003
hgdp	rs200040003
ensembl	rs200040003
geneview	rs200040003
scholar	rs200040003
google	rs200040003
pharmgkb	rs200040003
gwascentral	rs200040003
openSNP	rs200040003
23andMe	rs200040003
SNPshot	rs200040003
SNPdbe	rs200040003
MSV3d	rs200040003
GWAS Ctlg	rs200040003

Max Magnitude

0

ClinVar
Risk	rs200040003(T;T)
Alt	rs200040003(T;T)
Reference	Rs200040003(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CUL7
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.43014321C>T
CLNSRC
CLNACC	RCV000171398.1,