rs869320717

Orientation

minus

Stabilized

minus

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

Make rs869320717(-;-)

Make rs869320717(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

44309772

Gene

ALX4

is a	snp
is	mentioned by
dbSNP	rs869320717
dbSNP (classic)	rs869320717
ClinGen	rs869320717
ebi	rs869320717
HLI	rs869320717
Exac	rs869320717
Gnomad	rs869320717
Varsome	rs869320717
LitVar	rs869320717
Map	rs869320717
PheGenI	rs869320717
Biobank	rs869320717
1000 genomes	rs869320717
hgdp	rs869320717
ensembl	rs869320717
geneview	rs869320717
scholar	rs869320717
google	rs869320717
pharmgkb	rs869320717
gwascentral	rs869320717
openSNP	rs869320717
23andMe	rs869320717
SNPshot	rs869320717
SNPdbe	rs869320717
MSV3d	rs869320717
GWAS Ctlg	rs869320717

Max Magnitude

0

ClinVar
Risk	rs869320717(-;-)
Alt	rs869320717(-;-)
Reference	Rs869320717(G;G)
Significance	Pathogenic
Disease	Frontonasal dysplasia 2
Variation	info
Gene	ALX4
CLNDBN	Frontonasal dysplasia 2
Reversed	1
HGVS	NC_000011.9:g.44331322delC
CLNSRC
CLNACC	RCV000210924.1,