rs875989843

Orientation

plus

Stabilized

plus

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

Make rs875989843(A;A)

Make rs875989843(A;T)

Reference

GRCh38.p2 38.2/147

Chromosome

6

Position

168598828

Gene

SMOC2

is a	snp
is	mentioned by
dbSNP	rs875989843
dbSNP (classic)	rs875989843
ClinGen	rs875989843
ebi	rs875989843
HLI	rs875989843
Exac	rs875989843
Gnomad	rs875989843
Varsome	rs875989843
LitVar	rs875989843
Map	rs875989843
PheGenI	rs875989843
Biobank	rs875989843
1000 genomes	rs875989843
hgdp	rs875989843
ensembl	rs875989843
geneview	rs875989843
scholar	rs875989843
google	rs875989843
pharmgkb	rs875989843
gwascentral	rs875989843
openSNP	rs875989843
23andMe	rs875989843
SNPshot	rs875989843
SNPdbe	rs875989843
MSV3d	rs875989843
GWAS Ctlg	rs875989843

Max Magnitude

0

ClinVar
Risk	rs875989843(A;A)
Alt	rs875989843(A;A)
Reference	Rs875989843(T;T)
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.168999508T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000210957.1,