Have questions? Visit https://www.reddit.com/r/SNPedia

rs786200927

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786200927(G;T)
Make rs786200927(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position168441455
GeneSMOC2
is asnp
is mentioned by
dbSNPrs786200927
ebirs786200927
HLIrs786200927
Exacrs786200927
Varsomers786200927
Maprs786200927
PheGenIrs786200927
hapmaprs786200927
1000 genomesrs786200927
hgdprs786200927
ensemblrs786200927
gopubmedrs786200927
geneviewrs786200927
scholarrs786200927
googlers786200927
pharmgkbrs786200927
gwascentralrs786200927
openSNPrs786200927
23andMers786200927
23andMe allrs786200927
SNP Nexus

SNPshotrs786200927
SNPdbers786200927
MSV3drs786200927
GWAS Ctlgrs786200927
Max Magnitude0
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,