rs1057518987

Orientation

minus

Stabilized

minus

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

Make rs1057518987(-;-)

Make rs1057518987(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

89280324

Gene

ANKRD11

is a	snp
is	mentioned by
dbSNP	rs1057518987
dbSNP (classic)	rs1057518987
ClinGen	rs1057518987
ebi	rs1057518987
HLI	rs1057518987
Exac	rs1057518987
Gnomad	rs1057518987
Varsome	rs1057518987
LitVar	rs1057518987
Map	rs1057518987
PheGenI	rs1057518987
Biobank	rs1057518987
1000 genomes	rs1057518987
hgdp	rs1057518987
ensembl	rs1057518987
geneview	rs1057518987
scholar	rs1057518987
google	rs1057518987
pharmgkb	rs1057518987
gwascentral	rs1057518987
openSNP	rs1057518987
23andMe	rs1057518987
SNPshot	rs1057518987
SNPdbe	rs1057518987
MSV3d	rs1057518987
GWAS Ctlg	rs1057518987

Max Magnitude

0

ClinVar
Risk	rs1057518987(-;-)
Alt	rs1057518987(-;-)
Reference	Rs1057518987(C;C)
Significance	Probable-Pathogenic
Disease	Moderate intellectual deficiency
Variation	info
Gene	ANKRD11
CLNDBN	Moderate intellectual deficiency
Reversed	1
HGVS	NC_000016.9:g.89346732delG
CLNSRC
CLNACC	RCV000415439.1,