rs104894197

Orientation

minus

Stabilized

minus

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

Make rs104894197(A;A)

Make rs104894197(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

44275505

Gene

ALX4

is a	snp
is	mentioned by
dbSNP	rs104894197
dbSNP (classic)	rs104894197
ClinGen	rs104894197
ebi	rs104894197
HLI	rs104894197
Exac	rs104894197
Gnomad	rs104894197
Varsome	rs104894197
LitVar	rs104894197
Map	rs104894197
PheGenI	rs104894197
Biobank	rs104894197
1000 genomes	rs104894197
hgdp	rs104894197
ensembl	rs104894197
geneview	rs104894197
scholar	rs104894197
google	rs104894197
pharmgkb	rs104894197
gwascentral	rs104894197
openSNP	rs104894197
23andMe	rs104894197
SNPshot	rs104894197
SNPdbe	rs104894197
MSV3d	rs104894197
GWAS Ctlg	rs104894197

Max Magnitude

0

OMIM	605420
Desc
Variant	0006
Related	also

ClinVar
Risk	rs104894197(A;A) rs104894197(T;T)
Alt	rs104894197(A;A) rs104894197(T;T)
Reference	Rs104894197(C;C)
Significance	Pathogenic
Disease	Parietal foramina 2
Variation	info
Gene	ALX4
CLNDBN	Parietal foramina 2
Reversed	1
HGVS	NC_000011.9:g.44297055G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005321.4,