rs886039477

Orientation

minus

Stabilized

minus

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

Make rs886039477(-;-)

Make rs886039477(-;AA)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

89282771

Gene

ANKRD11

is a	snp
is	mentioned by
dbSNP	rs886039477
dbSNP (classic)	rs886039477
ClinGen	rs886039477
ebi	rs886039477
HLI	rs886039477
Exac	rs886039477
Gnomad	rs886039477
Varsome	rs886039477
LitVar	rs886039477
Map	rs886039477
PheGenI	rs886039477
Biobank	rs886039477
1000 genomes	rs886039477
hgdp	rs886039477
ensembl	rs886039477
geneview	rs886039477
scholar	rs886039477
google	rs886039477
pharmgkb	rs886039477
gwascentral	rs886039477
openSNP	rs886039477
23andMe	rs886039477
SNPshot	rs886039477
SNPdbe	rs886039477
MSV3d	rs886039477
GWAS Ctlg	rs886039477

Max Magnitude

0

ClinVar
Risk	rs886039477(-;-)
Alt	rs886039477(-;-)
Reference	Rs886039477(AA;AA)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ANKRD11
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.89349179_89349180delTT
CLNSRC
CLNACC	RCV000256105.1,