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rs730882118

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730882118(A;A)
Make rs730882118(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position160172665
GeneITGB6
is asnp
is mentioned by
dbSNPrs730882118
ebirs730882118
HLIrs730882118
Exacrs730882118
Varsomers730882118
Maprs730882118
PheGenIrs730882118
hapmaprs730882118
1000 genomesrs730882118
hgdprs730882118
ensemblrs730882118
gopubmedrs730882118
geneviewrs730882118
scholarrs730882118
googlers730882118
pharmgkbrs730882118
gwascentralrs730882118
openSNPrs730882118
23andMers730882118
23andMe allrs730882118
SNP Nexus

SNPshotrs730882118
SNPdbers730882118
MSV3drs730882118
GWAS Ctlgrs730882118
Max Magnitude0
ClinVar
Risk rs730882118(A;A)
Alt rs730882118(A;A)
Reference rs730882118(T;T)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene ITGB6
CLNDBN Amelogenesis imperfecta, type IH
Reversed 1
HGVS NC_000002.11:g.161029176A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000157639.3,