rs104893850

Orientation

plus

Stabilized

plus

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

Make rs104893850(C;T)

Make rs104893850(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

4862808

Gene

MSX1

is a	snp
is	mentioned by
dbSNP	rs104893850
dbSNP (classic)	rs104893850
ClinGen	rs104893850
ebi	rs104893850
HLI	rs104893850
Exac	rs104893850
Gnomad	rs104893850
Varsome	rs104893850
LitVar	rs104893850
Map	rs104893850
PheGenI	rs104893850
Biobank	rs104893850
1000 genomes	rs104893850
hgdp	rs104893850
ensembl	rs104893850
geneview	rs104893850
scholar	rs104893850
google	rs104893850
pharmgkb	rs104893850
gwascentral	rs104893850
openSNP	rs104893850
23andMe	rs104893850
SNPshot	rs104893850
SNPdbe	rs104893850
MSV3d	rs104893850
GWAS Ctlg	rs104893850

Max Magnitude

0

OMIM	142983
Desc
Variant	0006
Related	also

ClinVar
Risk	rs104893850(T;T)
Alt	rs104893850(T;T)
Reference	Rs104893850(C;C)
Significance	Pathogenic
Disease	Selective tooth agenesis 1
Variation	info
Gene	MSX1
CLNDBN	Selective tooth agenesis 1
Reversed	0
HGVS	NC_000004.11:g.4864535C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016010.26,