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rs786201004

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786201004(-;-)
Make rs786201004(-;G)
Make rs786201004(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position209615395
GeneLAMB3
is asnp
is mentioned by
dbSNPrs786201004
ebirs786201004
HLIrs786201004
Exacrs786201004
Varsomers786201004
Maprs786201004
PheGenIrs786201004
hapmaprs786201004
1000 genomesrs786201004
hgdprs786201004
ensemblrs786201004
gopubmedrs786201004
geneviewrs786201004
scholarrs786201004
googlers786201004
pharmgkbrs786201004
gwascentralrs786201004
openSNPrs786201004
23andMers786201004
23andMe allrs786201004
SNP Nexus

SNPshotrs786201004
SNPdbers786201004
MSV3drs786201004
GWAS Ctlgrs786201004
Max Magnitude0
ClinVar
Risk rs786201004(G;G)
Alt rs786201004(G;G)
Reference rs786201004(;)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene LAMB3
CLNDBN Amelogenesis imperfecta, type IA
Reversed 1
HGVS NC_000001.10:g.209788741dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000157637.4,