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

rs869320671

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869320671(A;A)
Make rs869320671(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position209615359
GeneLAMB3
is asnp
is mentioned by
dbSNPrs869320671
ebirs869320671
HLIrs869320671
Exacrs869320671
Varsomers869320671
Maprs869320671
PheGenIrs869320671
hapmaprs869320671
1000 genomesrs869320671
hgdprs869320671
ensemblrs869320671
gopubmedrs869320671
geneviewrs869320671
scholarrs869320671
googlers869320671
pharmgkbrs869320671
gwascentralrs869320671
openSNPrs869320671
23andMers869320671
23andMe allrs869320671
SNP Nexus

SNPshotrs869320671
SNPdbers869320671
MSV3drs869320671
GWAS Ctlgrs869320671
Max Magnitude0
ClinVar
Risk rs869320671(A;A)
Alt rs869320671(A;A)
Reference rs869320671(C;C)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene LAMB3
CLNDBN Amelogenesis imperfecta, type IA
Reversed 1
HGVS NC_000001.10:g.209788704G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000157636.3,