rs863223319

Orientation

minus

Stabilized

minus

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

Make rs863223319(C;C)

Make rs863223319(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

89274958

Gene

ANKRD11

is a	snp
is	mentioned by
dbSNP	rs863223319
dbSNP (classic)	rs863223319
ClinGen	rs863223319
ebi	rs863223319
HLI	rs863223319
Exac	rs863223319
Gnomad	rs863223319
Varsome	rs863223319
LitVar	rs863223319
Map	rs863223319
PheGenI	rs863223319
Biobank	rs863223319
1000 genomes	rs863223319
hgdp	rs863223319
ensembl	rs863223319
geneview	rs863223319
scholar	rs863223319
google	rs863223319
pharmgkb	rs863223319
gwascentral	rs863223319
openSNP	rs863223319
23andMe	rs863223319
SNPshot	rs863223319
SNPdbe	rs863223319
MSV3d	rs863223319
GWAS Ctlg	rs863223319

Max Magnitude

0

ClinVar
Risk	rs863223319(A;A) rs863223319(C;C)
Alt	rs863223319(A;A) rs863223319(C;C)
Reference	Rs863223319(G;G)
Significance	Pathogenic
Disease	KBG syndrome not provided
Variation	info
Gene	ANKRD11
CLNDBN	KBG syndrome not provided
Reversed	1
HGVS	NC_000016.9:g.89341366C>G; NC_000016.9:g.89341366C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023875.3, RCV000418665.1,