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rs786205094

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205094(-;-)
Make rs786205094(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position209630654
GeneLAMB3
is asnp
is mentioned by
dbSNPrs786205094
ebirs786205094
HLIrs786205094
Exacrs786205094
Varsomers786205094
Maprs786205094
PheGenIrs786205094
hapmaprs786205094
1000 genomesrs786205094
hgdprs786205094
ensemblrs786205094
gopubmedrs786205094
geneviewrs786205094
scholarrs786205094
googlers786205094
pharmgkbrs786205094
gwascentralrs786205094
openSNPrs786205094
23andMers786205094
23andMe allrs786205094
SNP Nexus

SNPshotrs786205094
SNPdbers786205094
MSV3drs786205094
GWAS Ctlgrs786205094
Max Magnitude0
ClinVar
Risk rs786205094(;)
Alt rs786205094(;)
Reference rs786205094(T;T)
Significance Pathogenic
Disease Adult junctional epidermolysis bullosa
Variation info
Gene LAMB3
CLNDBN Adult junctional epidermolysis bullosa
Reversed 1
HGVS NC_000001.10:g.209803999delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000015643.23,