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rs146794392

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs146794392(A;A)
Make rs146794392(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position209623999
GeneLAMB3, MIR4260
is asnp
is mentioned by
dbSNPrs146794392
ebirs146794392
HLIrs146794392
Exacrs146794392
Varsomers146794392
Maprs146794392
PheGenIrs146794392
hapmaprs146794392
1000 genomesrs146794392
hgdprs146794392
ensemblrs146794392
gopubmedrs146794392
geneviewrs146794392
scholarrs146794392
googlers146794392
pharmgkbrs146794392
gwascentralrs146794392
openSNPrs146794392
23andMers146794392
23andMe allrs146794392
SNP Nexus

SNPshotrs146794392
SNPdbers146794392
MSV3drs146794392
GWAS Ctlgrs146794392
Max Magnitude0
ClinVar
Risk rs146794392(A;A)
Alt rs146794392(A;A)
Reference rs146794392(G;G)
Significance Probable-Pathogenic
Disease Junctional epidermolysis bullosa gravis of Herlitz
Variation info
Gene MIR4260 LAMB3
CLNDBN Junctional epidermolysis bullosa gravis of Herlitz
Reversed 0
HGVS NC_000001.10:g.209797344G>A
CLNSRC
CLNACC RCV000169424.1,