rs797044900

Orientation

minus

Stabilized

minus

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

Make rs797044900(C;T)

Make rs797044900(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

89268645

Gene

ANKRD11

is a	snp
is	mentioned by
dbSNP	rs797044900
dbSNP (classic)	rs797044900
ClinGen	rs797044900
ebi	rs797044900
HLI	rs797044900
Exac	rs797044900
Gnomad	rs797044900
Varsome	rs797044900
LitVar	rs797044900
Map	rs797044900
PheGenI	rs797044900
Biobank	rs797044900
1000 genomes	rs797044900
hgdp	rs797044900
ensembl	rs797044900
geneview	rs797044900
scholar	rs797044900
google	rs797044900
pharmgkb	rs797044900
gwascentral	rs797044900
openSNP	rs797044900
23andMe	rs797044900
SNPshot	rs797044900
SNPdbe	rs797044900
MSV3d	rs797044900
GWAS Ctlg	rs797044900

Max Magnitude

0

ClinVar
Risk	rs797044900(T;T)
Alt	rs797044900(T;T)
Reference	Rs797044900(C;C)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	LOC101927838 ANKRD11
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000016.9:g.89335053G>A
CLNSRC
CLNACC	RCV000190724.1,