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rs730880298

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880298(A;A)
Make rs730880298(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position160195376
GeneITGB6
is asnp
is mentioned by
dbSNPrs730880298
ebirs730880298
HLIrs730880298
Exacrs730880298
Varsomers730880298
Maprs730880298
PheGenIrs730880298
hapmaprs730880298
1000 genomesrs730880298
hgdprs730880298
ensemblrs730880298
gopubmedrs730880298
geneviewrs730880298
scholarrs730880298
googlers730880298
pharmgkbrs730880298
gwascentralrs730880298
openSNPrs730880298
23andMers730880298
23andMe allrs730880298
SNP Nexus

SNPshotrs730880298
SNPdbers730880298
MSV3drs730880298
GWAS Ctlgrs730880298
Max Magnitude0
ClinVar
Risk rs730880298(A;A)
Alt rs730880298(A;A)
Reference rs730880298(C;C)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene ITGB6
CLNDBN Amelogenesis imperfecta, type IH
Reversed 1
HGVS NC_000002.11:g.161051887G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000157641.3,