rs267606653

Orientation

minus

Stabilized

minus

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

Make rs267606653(C;T)

Make rs267606653(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

44267607

Gene

ALX4

is a	snp
is	mentioned by
dbSNP	rs267606653
dbSNP (classic)	rs267606653
ClinGen	rs267606653
ebi	rs267606653
HLI	rs267606653
Exac	rs267606653
Gnomad	rs267606653
Varsome	rs267606653
LitVar	rs267606653
Map	rs267606653
PheGenI	rs267606653
Biobank	rs267606653
1000 genomes	rs267606653
hgdp	rs267606653
ensembl	rs267606653
geneview	rs267606653
scholar	rs267606653
google	rs267606653
pharmgkb	rs267606653
gwascentral	rs267606653
openSNP	rs267606653
23andMe	rs267606653
SNPshot	rs267606653
SNPdbe	rs267606653
MSV3d	rs267606653
GWAS Ctlg	rs267606653

Max Magnitude

0

ClinVar
Risk	rs267606653(T;T)
Alt	rs267606653(T;T)
Reference	Rs267606653(C;C)
Significance	Pathogenic
Disease	Frontonasal dysplasia 2
Variation	info
Gene	ALX4
CLNDBN	Frontonasal dysplasia 2
Reversed	1
HGVS	NC_000011.9:g.44289157G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005323.3,