rs12421995

Orientation

plus

Stabilized

plus

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

Make rs12421995(A;A)

Make rs12421995(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

44309759

Gene

ALX4

is a	snp
is	mentioned by
dbSNP	rs12421995
dbSNP (classic)	rs12421995
ClinGen	rs12421995
ebi	rs12421995
HLI	rs12421995
Exac	rs12421995
Gnomad	rs12421995
Varsome	rs12421995
LitVar	rs12421995
Map	rs12421995
PheGenI	rs12421995
Biobank	rs12421995
1000 genomes	rs12421995
hgdp	rs12421995
ensembl	rs12421995
geneview	rs12421995
scholar	rs12421995
google	rs12421995
pharmgkb	rs12421995
gwascentral	rs12421995
openSNP	rs12421995
23andMe	rs12421995
SNPshot	rs12421995
SNPdbe	rs12421995
MSV3d	rs12421995
GWAS Ctlg	rs12421995

GMAF

0.3636

Max Magnitude

0

[PMID 16319823] Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.

ClinVar
Risk	rs12421995(A;A)
Alt	rs12421995(A;A)
Reference	Rs12421995(G;G)
Significance	Non-pathogenic
Disease	Enlarged parietal foramina
Variation	info
Gene	ALX4
CLNDBN	Enlarged parietal foramina
Reversed	0
HGVS	NC_000011.9:g.44331309G>A
CLNSRC
CLNACC	RCV000282185.1,

[PMID 12774039] Clinical and molecular analysis of nine families with Adams-Oliver syndrome.