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rs267607178

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607178(C;G)
Make rs267607178(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position53615858
GeneWDR72
is asnp
is mentioned by
dbSNPrs267607178
ebirs267607178
HLIrs267607178
Exacrs267607178
Varsomers267607178
Maprs267607178
PheGenIrs267607178
hapmaprs267607178
1000 genomesrs267607178
hgdprs267607178
ensemblrs267607178
gopubmedrs267607178
geneviewrs267607178
scholarrs267607178
googlers267607178
pharmgkbrs267607178
gwascentralrs267607178
openSNPrs267607178
23andMers267607178
23andMe allrs267607178
SNP Nexus

SNPshotrs267607178
SNPdbers267607178
MSV3drs267607178
GWAS Ctlgrs267607178
Max Magnitude0
ClinVar
Risk rs267607178(G;G)
Alt rs267607178(G;G)
Reference rs267607178(C;C)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene WDR72
CLNDBN Amelogenesis imperfecta, hypomaturation type, IIA3
Reversed 1
HGVS NC_000015.9:g.53908055G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000255.3,