rs104894191

Orientation

minus

Stabilized

minus

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

Make rs104894191(C;T)

Make rs104894191(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

44309645

Gene

ALX4

is a	snp
is	mentioned by
dbSNP	rs104894191
dbSNP (classic)	rs104894191
ClinGen	rs104894191
ebi	rs104894191
HLI	rs104894191
Exac	rs104894191
Gnomad	rs104894191
Varsome	rs104894191
LitVar	rs104894191
Map	rs104894191
PheGenI	rs104894191
Biobank	rs104894191
1000 genomes	rs104894191
hgdp	rs104894191
ensembl	rs104894191
geneview	rs104894191
scholar	rs104894191
google	rs104894191
pharmgkb	rs104894191
gwascentral	rs104894191
openSNP	rs104894191
23andMe	rs104894191
SNPshot	rs104894191
SNPdbe	rs104894191
MSV3d	rs104894191
GWAS Ctlg	rs104894191

Max Magnitude

0

OMIM	605420
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894191(T;T)
Alt	rs104894191(T;T)
Reference	Rs104894191(C;C)
Significance	Pathogenic
Disease	Parietal foramina 2
Variation	info
Gene	ALX4
CLNDBN	Parietal foramina 2
Reversed	1
HGVS	NC_000011.9:g.44331195G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005316.4,