rs587777701

Orientation

plus

Stabilized

minus

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

Make rs587777701(C;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

44275452

Gene

ALX4

is a	snp
is	mentioned by
dbSNP	rs587777701
dbSNP (classic)	rs587777701
ClinGen	rs587777701
ebi	rs587777701
HLI	rs587777701
Exac	rs587777701
Gnomad	rs587777701
Varsome	rs587777701
LitVar	rs587777701
Map	rs587777701
PheGenI	rs587777701
Biobank	rs587777701
1000 genomes	rs587777701
hgdp	rs587777701
ensembl	rs587777701
geneview	rs587777701
scholar	rs587777701
google	rs587777701
pharmgkb	rs587777701
gwascentral	rs587777701
openSNP	rs587777701
23andMe	rs587777701
SNPshot	rs587777701
SNPdbe	rs587777701
MSV3d	rs587777701
GWAS Ctlg	rs587777701

Max Magnitude

0

ClinVar
Risk	Rs587777701(G;G)
Alt	Rs587777701(G;G)
Reference	Rs587777701(C;C)
Significance	Pathogenic
Disease	Frontonasal dysplasia 2
Variation	info
Gene	ALX4
CLNDBN	Frontonasal dysplasia 2
Reversed	1
HGVS	NC_000011.9:g.44297002G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000144037.2,