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rs587776588

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776588(-;-)
Make rs587776588(-;AG)
Make rs587776588(AG;AG)
ReferenceGRCh38 38.1/142
Chromosome4
Position70642685
GeneENAM
is asnp
is mentioned by
dbSNPrs587776588
ebirs587776588
HLIrs587776588
Exacrs587776588
Varsomers587776588
Maprs587776588
PheGenIrs587776588
hapmaprs587776588
1000 genomesrs587776588
hgdprs587776588
ensemblrs587776588
gopubmedrs587776588
geneviewrs587776588
scholarrs587776588
googlers587776588
pharmgkbrs587776588
gwascentralrs587776588
openSNPrs587776588
23andMers587776588
23andMe allrs587776588
SNP Nexus

SNPshotrs587776588
SNPdbers587776588
MSV3drs587776588
GWAS Ctlgrs587776588
Max Magnitude0
ClinVar
Risk rs587776588(AG;AG)
Alt rs587776588(AG;AG)
Reference rs587776588(;)
Significance Other
Disease Amelogenesis imperfecta Amelogenesis imperfecta - hypoplastic autosomal dominant - local
Variation info
Gene ENAM
CLNDBN Amelogenesis imperfecta, type IC Amelogenesis imperfecta - hypoplastic autosomal dominant - local
Reversed 0
HGVS NC_000004.11:g.71508402_71508403insAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000004460.5, RCV000144087.2,