rs121908168

Orientation

minus

Stabilized

minus

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

Make rs121908168(C;T)

Make rs121908168(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

110064634

Gene

ALX3

is a	snp
is	mentioned by
dbSNP	rs121908168
dbSNP (classic)	rs121908168
ClinGen	rs121908168
ebi	rs121908168
HLI	rs121908168
Exac	rs121908168
Gnomad	rs121908168
Varsome	rs121908168
LitVar	rs121908168
Map	rs121908168
PheGenI	rs121908168
Biobank	rs121908168
1000 genomes	rs121908168
hgdp	rs121908168
ensembl	rs121908168
geneview	rs121908168
scholar	rs121908168
google	rs121908168
pharmgkb	rs121908168
gwascentral	rs121908168
openSNP	rs121908168
23andMe	rs121908168
SNPshot	rs121908168
SNPdbe	rs121908168
MSV3d	rs121908168
GWAS Ctlg	rs121908168

Max Magnitude

0

OMIM	606014
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121908168(T;T)
Alt	rs121908168(T;T)
Reference	Rs121908168(C;C)
Significance	Pathogenic
Disease	Frontonasal dysplasia 1
Variation	info
Gene	ALX3
CLNDBN	Frontonasal dysplasia 1
Reversed	1
HGVS	NC_000001.10:g.110607256G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004908.3,