rs199800166

Orientation

plus

Stabilized

plus

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

Make rs199800166(C;T)

Make rs199800166(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

89283858

Gene

ANKRD11

is a	snp
is	mentioned by
dbSNP	rs199800166
dbSNP (classic)	rs199800166
ClinGen	rs199800166
ebi	rs199800166
HLI	rs199800166
Exac	rs199800166
Gnomad	rs199800166
Varsome	rs199800166
LitVar	rs199800166
Map	rs199800166
PheGenI	rs199800166
Biobank	rs199800166
1000 genomes	rs199800166
hgdp	rs199800166
ensembl	rs199800166
geneview	rs199800166
scholar	rs199800166
google	rs199800166
pharmgkb	rs199800166
gwascentral	rs199800166
openSNP	rs199800166
23andMe	rs199800166
SNPshot	rs199800166
SNPdbe	rs199800166
MSV3d	rs199800166
GWAS Ctlg	rs199800166

Max Magnitude

0

ClinVar
Risk	rs199800166(T;T)
Alt	rs199800166(T;T)
Reference	Rs199800166(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ANKRD11
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.89350266C>T
CLNSRC
CLNACC	RCV000493061.1,