rs886039600

Orientation

plus

Stabilized

plus

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

Make rs886039600(A;G)

Make rs886039600(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

67621454

Gene

CTCF

is a	snp
is	mentioned by
dbSNP	rs886039600
dbSNP (classic)	rs886039600
ClinGen	rs886039600
ebi	rs886039600
HLI	rs886039600
Exac	rs886039600
Gnomad	rs886039600
Varsome	rs886039600
LitVar	rs886039600
Map	rs886039600
PheGenI	rs886039600
Biobank	rs886039600
1000 genomes	rs886039600
hgdp	rs886039600
ensembl	rs886039600
geneview	rs886039600
scholar	rs886039600
google	rs886039600
pharmgkb	rs886039600
gwascentral	rs886039600
openSNP	rs886039600
23andMe	rs886039600
SNPshot	rs886039600
SNPdbe	rs886039600
MSV3d	rs886039600
GWAS Ctlg	rs886039600

Max Magnitude

0

ClinVar
Risk	rs886039600(G;G)
Alt	rs886039600(G;G)
Reference	Rs886039600(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CTCF
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.67655357A>G
CLNSRC
CLNACC	RCV000255519.1,