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rs146645381

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs146645381(A;A)
Make rs146645381(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position75564364
GeneC4orf26
is asnp
is mentioned by
dbSNPrs146645381
ebirs146645381
HLIrs146645381
Exacrs146645381
Varsomers146645381
Maprs146645381
PheGenIrs146645381
hapmaprs146645381
1000 genomesrs146645381
hgdprs146645381
ensemblrs146645381
gopubmedrs146645381
geneviewrs146645381
scholarrs146645381
googlers146645381
pharmgkbrs146645381
gwascentralrs146645381
openSNPrs146645381
23andMers146645381
23andMe allrs146645381
SNP Nexus

SNPshotrs146645381
SNPdbers146645381
MSV3drs146645381
GWAS Ctlgrs146645381
Max Magnitude0
ClinVar
Risk rs146645381(A;A)
Alt rs146645381(A;A)
Reference rs146645381(G;G)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene C4orf26
CLNDBN Amelogenesis imperfecta, hypomaturation type IIA4
Reversed 0
HGVS NC_000004.11:g.76489574G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030794.2,