rs886039902

Orientation

minus

Stabilized

minus

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

Make rs886039902(-;-)

Make rs886039902(-;AAAAA)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

89284130

Gene

ANKRD11

is a	snp
is	mentioned by
dbSNP	rs886039902
dbSNP (classic)	rs886039902
ClinGen	rs886039902
ebi	rs886039902
HLI	rs886039902
Exac	rs886039902
Gnomad	rs886039902
Varsome	rs886039902
LitVar	rs886039902
Map	rs886039902
PheGenI	rs886039902
Biobank	rs886039902
1000 genomes	rs886039902
hgdp	rs886039902
ensembl	rs886039902
geneview	rs886039902
scholar	rs886039902
google	rs886039902
pharmgkb	rs886039902
gwascentral	rs886039902
openSNP	rs886039902
23andMe	rs886039902
SNPshot	rs886039902
SNPdbe	rs886039902
MSV3d	rs886039902
GWAS Ctlg	rs886039902

Max Magnitude

0

ClinVar
Risk	rs886039902(-;-)
Alt	rs886039902(-;-)
Reference	Rs886039902(AAAAA;AAAAA)
Significance	Pathogenic
Disease	KBG syndrome
Variation	info
Gene	ANKRD11
CLNDBN	KBG syndrome
Reversed	1
HGVS	NC_000016.9:g.89350538_89350542delTTTTT
CLNSRC
CLNACC	RCV000256444.1,