rs1057520565

Orientation

minus

Stabilized

minus

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

Make rs1057520565(C;T)

Make rs1057520565(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

89279404

Gene

ANKRD11

is a	snp
is	mentioned by
dbSNP	rs1057520565
dbSNP (classic)	rs1057520565
ClinGen	rs1057520565
ebi	rs1057520565
HLI	rs1057520565
Exac	rs1057520565
Gnomad	rs1057520565
Varsome	rs1057520565
LitVar	rs1057520565
Map	rs1057520565
PheGenI	rs1057520565
Biobank	rs1057520565
1000 genomes	rs1057520565
hgdp	rs1057520565
ensembl	rs1057520565
geneview	rs1057520565
scholar	rs1057520565
google	rs1057520565
pharmgkb	rs1057520565
gwascentral	rs1057520565
openSNP	rs1057520565
23andMe	rs1057520565
SNPshot	rs1057520565
SNPdbe	rs1057520565
MSV3d	rs1057520565
GWAS Ctlg	rs1057520565

Max Magnitude

0

ClinVar
Risk	rs1057520565(T;T)
Alt	rs1057520565(T;T)
Reference	Rs1057520565(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ANKRD11
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.89345812G>A
CLNSRC
CLNACC	RCV000425698.1,