Have questions? Visit https://www.reddit.com/r/SNPedia

rs137854437

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854437(G;T)
Make rs137854437(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position143728218
GeneFAM83H
is asnp
is mentioned by
dbSNPrs137854437
ebirs137854437
HLIrs137854437
Exacrs137854437
Varsomers137854437
Maprs137854437
PheGenIrs137854437
hapmaprs137854437
1000 genomesrs137854437
hgdprs137854437
ensemblrs137854437
gopubmedrs137854437
geneviewrs137854437
scholarrs137854437
googlers137854437
pharmgkbrs137854437
gwascentralrs137854437
openSNPrs137854437
23andMers137854437
23andMe allrs137854437
SNP Nexus

SNPshotrs137854437
SNPdbers137854437
MSV3drs137854437
GWAS Ctlgrs137854437
Max Magnitude0
OMIM611927
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137854437(A,T;A,T)
Alt rs137854437(A,T;A,T)
Reference rs137854437(G;G)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene FAM83H
CLNDBN Amelogenesis imperfecta, hypocalcification type
Reversed 1
HGVS NC_000008.10:g.144810388C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000808.2,