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

rs869320747

From SNPedia

Orientationminus
Geno Mag Summary
(GACTGGAG;GACTGGAG) 0 common in clinvar
Make rs869320747(-;-)
Make rs869320747(-;GACTGGAG)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position209615337
GeneLAMB3
is asnp
is mentioned by
dbSNPrs869320747
ebirs869320747
HLIrs869320747
Exacrs869320747
Varsomers869320747
Maprs869320747
PheGenIrs869320747
hapmaprs869320747
1000 genomesrs869320747
hgdprs869320747
ensemblrs869320747
gopubmedrs869320747
geneviewrs869320747
scholarrs869320747
googlers869320747
pharmgkbrs869320747
gwascentralrs869320747
openSNPrs869320747
23andMers869320747
23andMe allrs869320747
SNP Nexus

SNPshotrs869320747
SNPdbers869320747
MSV3drs869320747
GWAS Ctlgrs869320747
Max Magnitude0
ClinVar
Risk rs869320747(;)
Alt rs869320747(;)
Reference rs869320747(GACTGGAG;GACTGGAG)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene LAMB3
CLNDBN Amelogenesis imperfecta, type IA
Reversed 1
HGVS NC_000001.10:g.209788682_209788689delCTCCAGTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000157635.3,