rs786200927

Orientation

plus

Stabilized

plus

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

Make rs786200927(G;T)

Make rs786200927(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

168441455

Gene

SMOC2

is a	snp
is	mentioned by
dbSNP	rs786200927
dbSNP (classic)	rs786200927
ClinGen	rs786200927
ebi	rs786200927
HLI	rs786200927
Exac	rs786200927
Gnomad	rs786200927
Varsome	rs786200927
LitVar	rs786200927
Map	rs786200927
PheGenI	rs786200927
Biobank	rs786200927
1000 genomes	rs786200927
hgdp	rs786200927
ensembl	rs786200927
geneview	rs786200927
scholar	rs786200927
google	rs786200927
pharmgkb	rs786200927
gwascentral	rs786200927
openSNP	rs786200927
23andMe	rs786200927
SNPshot	rs786200927
SNPdbe	rs786200927
MSV3d	rs786200927
GWAS Ctlg	rs786200927

Max Magnitude

0

ClinVar
Risk	rs786200927(T;T)
Alt	rs786200927(T;T)
Reference	Rs786200927(G;G)
Significance	Pathogenic
Disease	Dentin dysplasia
Variation	info
Gene	SMOC2
CLNDBN	Dentin dysplasia, type I, with extreme microdontia and misshapen teeth
Reversed	0
HGVS	NC_000006.11:g.168842135G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023634.4,