rs121913130

Orientation

plus

Stabilized

plus

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

Make rs121913130(A;A)

Make rs121913130(A;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

4860099

Gene

MSX1

is a	snp
is	mentioned by
dbSNP	rs121913130
dbSNP (classic)	rs121913130
ClinGen	rs121913130
ebi	rs121913130
HLI	rs121913130
Exac	rs121913130
Gnomad	rs121913130
Varsome	rs121913130
LitVar	rs121913130
Map	rs121913130
PheGenI	rs121913130
Biobank	rs121913130
1000 genomes	rs121913130
hgdp	rs121913130
ensembl	rs121913130
geneview	rs121913130
scholar	rs121913130
google	rs121913130
pharmgkb	rs121913130
gwascentral	rs121913130
openSNP	rs121913130
23andMe	rs121913130
23andMe all	rs121913130
SNPshot	rs121913130
SNPdbe	rs121913130
MSV3d	rs121913130
GWAS Ctlg	rs121913130

Max Magnitude

0

OMIM	142983
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121913130(A;A)
Alt	rs121913130(A;A)
Reference	Rs121913130(T;T)
Significance	Pathogenic
Disease	Selective tooth agenesis 1
Variation	info
Gene	MSX1
CLNDBN	Selective tooth agenesis 1
Reversed	0
HGVS	NC_000004.11:g.4861826T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016015.22,