rs869312713

Orientation

minus

Stabilized

minus

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

Make rs869312713(G;T)

Make rs869312713(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

89280070

Gene

ANKRD11

is a	snp
is	mentioned by
dbSNP	rs869312713
dbSNP (classic)	rs869312713
ClinGen	rs869312713
ebi	rs869312713
HLI	rs869312713
Exac	rs869312713
Gnomad	rs869312713
Varsome	rs869312713
LitVar	rs869312713
Map	rs869312713
PheGenI	rs869312713
Biobank	rs869312713
1000 genomes	rs869312713
hgdp	rs869312713
ensembl	rs869312713
geneview	rs869312713
scholar	rs869312713
google	rs869312713
pharmgkb	rs869312713
gwascentral	rs869312713
openSNP	rs869312713
23andMe	rs869312713
SNPshot	rs869312713
SNPdbe	rs869312713
MSV3d	rs869312713
GWAS Ctlg	rs869312713

Max Magnitude

0

ClinVar
Risk	rs869312713(T;T)
Alt	rs869312713(T;T)
Reference	Rs869312713(G;G)
Significance	Pathogenic
Disease	KBG syndrome
Variation	info
Gene	ANKRD11
CLNDBN	KBG syndrome
Reversed	1
HGVS	NC_000016.9:g.89346478C>A
CLNSRC
CLNACC	RCV000209927.1,