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rs875989843

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs875989843(A;A)
Make rs875989843(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position168598828
GeneSMOC2
is asnp
is mentioned by
dbSNPrs875989843
ebirs875989843
HLIrs875989843
Exacrs875989843
Varsomers875989843
Maprs875989843
PheGenIrs875989843
hapmaprs875989843
1000 genomesrs875989843
hgdprs875989843
ensemblrs875989843
gopubmedrs875989843
geneviewrs875989843
scholarrs875989843
googlers875989843
pharmgkbrs875989843
gwascentralrs875989843
openSNPrs875989843
23andMers875989843
23andMe allrs875989843
SNP Nexus

SNPshotrs875989843
SNPdbers875989843
MSV3drs875989843
GWAS Ctlgrs875989843
Max Magnitude0
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,