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rs587777536

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777536(A;T)
Make rs587777536(T;T)
ReferenceGRCh38 38.1/142
Chromosome14
Position92486738
GeneSLC24A4
is asnp
is mentioned by
dbSNPrs587777536
ebirs587777536
HLIrs587777536
Exacrs587777536
Varsomers587777536
Maprs587777536
PheGenIrs587777536
hapmaprs587777536
1000 genomesrs587777536
hgdprs587777536
ensemblrs587777536
gopubmedrs587777536
geneviewrs587777536
scholarrs587777536
googlers587777536
pharmgkbrs587777536
gwascentralrs587777536
openSNPrs587777536
23andMers587777536
23andMe allrs587777536
SNP Nexus

SNPshotrs587777536
SNPdbers587777536
MSV3drs587777536
GWAS Ctlgrs587777536
Max Magnitude0
ClinVar
Risk rs587777536(T;T)
Alt rs587777536(T;T)
Reference rs587777536(A;A)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene SLC24A4
CLNDBN Amelogenesis imperfecta, hypomaturation type IIA5
Reversed 0
HGVS NC_000014.8:g.92953082A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000128622.2,