rs876657391

Orientation

minus

Stabilized

minus

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

Make rs876657391(-;-)

Make rs876657391(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

44275622

Gene

ALX4

is a	snp
is	mentioned by
dbSNP	rs876657391
dbSNP (classic)	rs876657391
ClinGen	rs876657391
ebi	rs876657391
HLI	rs876657391
Exac	rs876657391
Gnomad	rs876657391
Varsome	rs876657391
LitVar	rs876657391
Map	rs876657391
PheGenI	rs876657391
Biobank	rs876657391
1000 genomes	rs876657391
hgdp	rs876657391
ensembl	rs876657391
geneview	rs876657391
scholar	rs876657391
google	rs876657391
pharmgkb	rs876657391
gwascentral	rs876657391
openSNP	rs876657391
23andMe	rs876657391
SNPshot	rs876657391
SNPdbe	rs876657391
MSV3d	rs876657391
GWAS Ctlg	rs876657391

Max Magnitude

0

ClinVar
Risk	rs876657391(-;-)
Alt	rs876657391(-;-)
Reference	Rs876657391(C;C)
Significance	Pathogenic
Disease	Frontonasal dysplasia 2
Variation	info
Gene	ALX4
CLNDBN	Frontonasal dysplasia 2
Reversed	1
HGVS	NC_000011.9:g.44297172delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000170519.2,