rs886039713

Orientation

minus

Stabilized

minus

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

Make rs886039713(A;A)

Make rs886039713(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

89284890

Gene

ANKRD11

is a	snp
is	mentioned by
dbSNP	rs886039713
dbSNP (classic)	rs886039713
ClinGen	rs886039713
ebi	rs886039713
HLI	rs886039713
Exac	rs886039713
Gnomad	rs886039713
Varsome	rs886039713
LitVar	rs886039713
Map	rs886039713
PheGenI	rs886039713
Biobank	rs886039713
1000 genomes	rs886039713
hgdp	rs886039713
ensembl	rs886039713
geneview	rs886039713
scholar	rs886039713
google	rs886039713
pharmgkb	rs886039713
gwascentral	rs886039713
openSNP	rs886039713
23andMe	rs886039713
SNPshot	rs886039713
SNPdbe	rs886039713
MSV3d	rs886039713
GWAS Ctlg	rs886039713

Max Magnitude

0

ClinVar
Risk	rs886039713(A;A)
Alt	rs886039713(A;A)
Reference	Rs886039713(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ANKRD11
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.89351298C>T
CLNSRC
CLNACC	RCV000255814.1,