rs104894192

Orientation

minus

Stabilized

minus

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

Make rs104894192(C;T)

Make rs104894192(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

44275389

Gene

ALX4

is a	snp
is	mentioned by
dbSNP	rs104894192
dbSNP (classic)	rs104894192
ClinGen	rs104894192
ebi	rs104894192
HLI	rs104894192
Exac	rs104894192
Gnomad	rs104894192
Varsome	rs104894192
LitVar	rs104894192
Map	rs104894192
PheGenI	rs104894192
Biobank	rs104894192
1000 genomes	rs104894192
hgdp	rs104894192
ensembl	rs104894192
geneview	rs104894192
scholar	rs104894192
google	rs104894192
pharmgkb	rs104894192
gwascentral	rs104894192
openSNP	rs104894192
23andMe	rs104894192
SNPshot	rs104894192
SNPdbe	rs104894192
MSV3d	rs104894192
GWAS Ctlg	rs104894192

Max Magnitude

0

OMIM	605420
Desc
Variant	0002
Related	also

ClinVar
Risk	rs104894192(T;T)
Alt	rs104894192(T;T)
Reference	Rs104894192(C;C)
Significance	Pathogenic
Disease	Parietal foramina 2
Variation	info
Gene	ALX4
CLNDBN	Parietal foramina 2
Reversed	1
HGVS	NC_000011.9:g.44296939G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005317.4,