Have questions? Visit https://www.reddit.com/r/SNPedia

rs398123379

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123379(-;-)
Make rs398123379(-;A)
ReferenceGRCh38 38.1/141
Chromosome6
Position129438688
GeneLAMA2
is asnp
is mentioned by
dbSNPrs398123379
ebirs398123379
HLIrs398123379
Exacrs398123379
Varsomers398123379
Maprs398123379
PheGenIrs398123379
hapmaprs398123379
1000 genomesrs398123379
hgdprs398123379
ensemblrs398123379
gopubmedrs398123379
geneviewrs398123379
scholarrs398123379
googlers398123379
pharmgkbrs398123379
gwascentralrs398123379
openSNPrs398123379
23andMers398123379
23andMe allrs398123379
SNP Nexus

SNPshotrs398123379
SNPdbers398123379
MSV3drs398123379
GWAS Ctlgrs398123379
Max Magnitude0
ClinVar
Risk rs398123379(;)
Alt rs398123379(;)
Reference rs398123379(A;A)
Significance Pathogenic
Disease not provided Merosin deficient congenital muscular dystrophy
Variation info
Gene LAMA2
CLNDBN not provided Merosin deficient congenital muscular dystrophy
Reversed 0
HGVS NC_000006.11:g.129759833delA
CLNSRC ClinVar
CLNACC RCV000078783.3, RCV000178482.1,