rs515726227

Orientation

plus

Stabilized

plus

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

Make rs515726227(-;TA)

Make rs515726227(TA;TA)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

4863142

Gene

MSX1

is a	snp
is	mentioned by
dbSNP	rs515726227
dbSNP (classic)	rs515726227
ClinGen	rs515726227
ebi	rs515726227
HLI	rs515726227
Exac	rs515726227
Gnomad	rs515726227
Varsome	rs515726227
LitVar	rs515726227
Map	rs515726227
PheGenI	rs515726227
Biobank	rs515726227
1000 genomes	rs515726227
hgdp	rs515726227
ensembl	rs515726227
geneview	rs515726227
scholar	rs515726227
google	rs515726227
pharmgkb	rs515726227
gwascentral	rs515726227
openSNP	rs515726227
23andMe	rs515726227
SNPshot	rs515726227
SNPdbe	rs515726227
MSV3d	rs515726227
GWAS Ctlg	rs515726227

Max Magnitude

0

ClinVar
Risk	rs515726227(AT;AT)
Alt	rs515726227(AT;AT)
Reference	Rs515726227(-;-)
Significance	Pathogenic
Disease	Selective tooth agenesis 1
Variation	info
Gene	MSX1
CLNDBN	Selective tooth agenesis 1
Reversed	0
HGVS	NC_000004.11:g.4864868_4864869dupTA
CLNSRC	VariO
CLNACC	RCV000157079.1,