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rs140015315

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs140015315(C;T)
Make rs140015315(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position160195535
GeneITGB6
is asnp
is mentioned by
dbSNPrs140015315
ebirs140015315
HLIrs140015315
Exacrs140015315
Varsomers140015315
Maprs140015315
PheGenIrs140015315
hapmaprs140015315
1000 genomesrs140015315
hgdprs140015315
ensemblrs140015315
gopubmedrs140015315
geneviewrs140015315
scholarrs140015315
googlers140015315
pharmgkbrs140015315
gwascentralrs140015315
openSNPrs140015315
23andMers140015315
23andMe allrs140015315
SNP Nexus

SNPshotrs140015315
SNPdbers140015315
MSV3drs140015315
GWAS Ctlgrs140015315
Max Magnitude0
ClinVar
Risk rs140015315(T;T)
Alt rs140015315(T;T)
Reference rs140015315(C;C)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene ITGB6
CLNDBN Amelogenesis imperfecta, type IH
Reversed 0
HGVS NC_000002.11:g.161052046C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000157638.4,