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rs878852983

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878852983(G;G)
Make rs878852983(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position33789079
GeneLEMD2, LOC105375024
is asnp
is mentioned by
dbSNPrs878852983
ebirs878852983
HLIrs878852983
Exacrs878852983
Varsomers878852983
Maprs878852983
PheGenIrs878852983
hapmaprs878852983
1000 genomesrs878852983
hgdprs878852983
ensemblrs878852983
gopubmedrs878852983
geneviewrs878852983
scholarrs878852983
googlers878852983
pharmgkbrs878852983
gwascentralrs878852983
openSNPrs878852983
23andMers878852983
23andMe allrs878852983
SNP Nexus

SNPshotrs878852983
SNPdbers878852983
MSV3drs878852983
GWAS Ctlgrs878852983
Max Magnitude0
ClinVar
Risk rs878852983(G;G)
Alt rs878852983(G;G)
Reference rs878852983(T;T)
Significance Pathogenic
Disease Cataract Hutterite type
Variation info
Gene LEMD2
CLNDBN Cataract Hutterite type
Reversed 1
HGVS NC_000006.11:g.33756856A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000224057.1,