rs104893852

Orientation

plus

Stabilized

plus

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

Make rs104893852(A;A)

Make rs104893852(A;C)

Reference

GRCh38 38.1/141

Chromosome

4

Position

4860231

Gene

MSX1

is a	snp
is	mentioned by
dbSNP	rs104893852
dbSNP (classic)	rs104893852
ClinGen	rs104893852
ebi	rs104893852
HLI	rs104893852
Exac	rs104893852
Gnomad	rs104893852
Varsome	rs104893852
LitVar	rs104893852
Map	rs104893852
PheGenI	rs104893852
Biobank	rs104893852
1000 genomes	rs104893852
hgdp	rs104893852
ensembl	rs104893852
geneview	rs104893852
scholar	rs104893852
google	rs104893852
pharmgkb	rs104893852
gwascentral	rs104893852
openSNP	rs104893852
23andMe	rs104893852
SNPshot	rs104893852
SNPdbe	rs104893852
MSV3d	rs104893852
GWAS Ctlg	rs104893852

Max Magnitude

0

OMIM	142983
Desc
Variant	0002
Related	also

ClinVar
Risk	rs104893852(A;A)
Alt	rs104893852(A;A)
Reference	Rs104893852(C;C)
Significance	Pathogenic
Disease	Tooth agenesis
Variation	info
Gene	MSX1
CLNDBN	Tooth agenesis, selective, with or without orofacial cleft
Reversed	0
HGVS	NC_000004.11:g.4861958C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016009.26,