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rs28933096

From SNPedia

Merged intors121913574
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs28933096(A;A)
Make rs28933096(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position129190317
GeneLAMA2
is asnp
is mentioned by
dbSNPrs28933096
ebirs28933096
HLIrs28933096
Exacrs28933096
Varsomers28933096
Maprs28933096
PheGenIrs28933096
hapmaprs28933096
1000 genomesrs28933096
hgdprs28933096
ensemblrs28933096
gopubmedrs28933096
geneviewrs28933096
scholarrs28933096
googlers28933096
pharmgkbrs28933096
gwascentralrs28933096
openSNPrs28933096
23andMers28933096
23andMe allrs28933096
SNP Nexus

SNPshotrs28933096
SNPdbers28933096
MSV3drs28933096
GWAS Ctlgrs28933096
StatusMerged into rs121913574
Max Magnitude0
OMIM156225
DescMUSCULAR DYSTROPHY, CONGENITAL, DUE TO PARTIAL LAMA2 DEFICIENCY
Variant0010
Relatedalso