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rs776537364

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs776537364(-;-)
Make rs776537364(-;A)
Make rs776537364(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position209634547
GeneLAMB3
is asnp
is mentioned by
dbSNPrs776537364
ebirs776537364
HLIrs776537364
Exacrs776537364
Varsomers776537364
Maprs776537364
PheGenIrs776537364
hapmaprs776537364
1000 genomesrs776537364
hgdprs776537364
ensemblrs776537364
gopubmedrs776537364
geneviewrs776537364
scholarrs776537364
googlers776537364
pharmgkbrs776537364
gwascentralrs776537364
openSNPrs776537364
23andMers776537364
23andMe allrs776537364
SNP Nexus

SNPshotrs776537364
SNPdbers776537364
MSV3drs776537364
GWAS Ctlgrs776537364
Max Magnitude0
ClinVar
Risk rs776537364(A;A)
Alt rs776537364(A;A)
Reference rs776537364(;)
Significance Probable-Pathogenic
Disease Junctional epidermolysis bullosa gravis of Herlitz
Variation info
Gene LAMB3
CLNDBN Junctional epidermolysis bullosa gravis of Herlitz
Reversed 0
HGVS NC_000001.10:g.209807893dupA
CLNSRC
CLNACC RCV000169311.1,