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rs606231462

From SNPedia

Orientationminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs606231462(-;-)
Make rs606231462(-;AT)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position53702235
GeneWDR72
is asnp
is mentioned by
dbSNPrs606231462
ebirs606231462
HLIrs606231462
Exacrs606231462
Varsomers606231462
Maprs606231462
PheGenIrs606231462
hapmaprs606231462
1000 genomesrs606231462
hgdprs606231462
ensemblrs606231462
gopubmedrs606231462
geneviewrs606231462
scholarrs606231462
googlers606231462
pharmgkbrs606231462
gwascentralrs606231462
openSNPrs606231462
23andMers606231462
23andMe allrs606231462
SNP Nexus

SNPshotrs606231462
SNPdbers606231462
MSV3drs606231462
GWAS Ctlgrs606231462
Max Magnitude0
ClinVar
Risk rs606231462(;)
Alt rs606231462(;)
Reference rs606231462(AT;AT)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene WDR72
CLNDBN Amelogenesis imperfecta, hypomaturation type, IIA3
Reversed 1
HGVS NC_000015.9:g.53994432_53994433delAT
CLNSRC OMIM Allelic Variant
CLNACC RCV000148931.3,