rs886041997

Orientation

plus

Stabilized

plus

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

Chromosome

16

Position

67611442

Gene

CTCF

is a	snp
is	mentioned by
dbSNP	rs886041997
dbSNP (classic)	rs886041997
ClinGen	rs886041997
ebi	rs886041997
HLI	rs886041997
Exac	rs886041997
Gnomad	rs886041997
Varsome	rs886041997
LitVar	rs886041997
Map	rs886041997
PheGenI	rs886041997
Biobank	rs886041997
1000 genomes	rs886041997
hgdp	rs886041997
ensembl	rs886041997
geneview	rs886041997
scholar	rs886041997
google	rs886041997
pharmgkb	rs886041997
gwascentral	rs886041997
openSNP	rs886041997
23andMe	rs886041997
SNPshot	rs886041997
SNPdbe	rs886041997
MSV3d	rs886041997
GWAS Ctlg	rs886041997

Max Magnitude

0

ClinVar
Risk	rs886041997(A;A)
Alt	rs886041997(A;A)
Reference	Rs886041997(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CTCF
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.67645345dupA
CLNSRC
CLNACC	RCV000398560.1,