rs104894196

Orientation

minus

Stabilized

minus

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

Make rs104894196(C;C)

Make rs104894196(C;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

44267585

Gene

ALX4

is a	snp
is	mentioned by
dbSNP	rs104894196
dbSNP (classic)	rs104894196
ClinGen	rs104894196
ebi	rs104894196
HLI	rs104894196
Exac	rs104894196
Gnomad	rs104894196
Varsome	rs104894196
LitVar	rs104894196
Map	rs104894196
PheGenI	rs104894196
Biobank	rs104894196
1000 genomes	rs104894196
hgdp	rs104894196
ensembl	rs104894196
geneview	rs104894196
scholar	rs104894196
google	rs104894196
pharmgkb	rs104894196
gwascentral	rs104894196
openSNP	rs104894196
23andMe	rs104894196
SNPshot	rs104894196
SNPdbe	rs104894196
MSV3d	rs104894196
GWAS Ctlg	rs104894196

Max Magnitude

0

OMIM	605420
Desc
Variant	0005
Related	also

ClinVar
Risk	rs104894196(C;C)
Alt	rs104894196(C;C)
Reference	Rs104894196(G;G)
Significance	Pathogenic
Disease	Parietal foramina 2
Variation	info
Gene	ALX4
CLNDBN	Parietal foramina 2
Reversed	1
HGVS	NC_000011.9:g.44289135C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005320.4,