rs797044890

Orientation

minus

Stabilized

minus

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

Make rs797044890(A;A)

Make rs797044890(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

89275092

Gene

ANKRD11

is a	snp
is	mentioned by
dbSNP	rs797044890
dbSNP (classic)	rs797044890
ClinGen	rs797044890
ebi	rs797044890
HLI	rs797044890
Exac	rs797044890
Gnomad	rs797044890
Varsome	rs797044890
LitVar	rs797044890
Map	rs797044890
PheGenI	rs797044890
Biobank	rs797044890
1000 genomes	rs797044890
hgdp	rs797044890
ensembl	rs797044890
geneview	rs797044890
scholar	rs797044890
google	rs797044890
pharmgkb	rs797044890
gwascentral	rs797044890
openSNP	rs797044890
23andMe	rs797044890
SNPshot	rs797044890
SNPdbe	rs797044890
MSV3d	rs797044890
GWAS Ctlg	rs797044890

Max Magnitude

0

ClinVar
Risk	rs797044890(A;A)
Alt	rs797044890(A;A)
Reference	Rs797044890(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases not provided
Variation	info
Gene	ANKRD11
CLNDBN	Inborn genetic diseases not provided
Reversed	1
HGVS	NC_000016.9:g.89341500C>T
CLNSRC
CLNACC	RCV000190712.1, RCV000335440.1,